Performance and Safety of the ANTALGEEK® Thess Monitoring Medical Device in the Outpatient Management of Acute Pain and Postoperative Recovery (TRACE)
2026年7月6日 更新者：Centre Hospitalier Universitaire de Nīmes
Evaluation of the Performance and Safety of the ANTALGEEK® Thess Monitoring Medical Device in the Outpatient Management of Acute Pain and Postoperative Recovery - A Single-Center, Randomized, Controlled Proof-of-Concept Study.
Acute postoperative pain (APOP) is a major public health problem, affecting nearly 10 million patients in France each year.
Effective analgesic therapy in the first postoperative week is a key factor in reducing early postoperative morbidity and mortality.
Poorly controlled APOP is a major risk factor for chronic postoperative pain.
In France today, more and more patients undergo surgical procedures as outpatients.
The challenge is to manage postoperative pain in the homes of patients who have undergone increasingly complex surgical procedures, either after outpatient surgery or after a prompt return home as part of an Enhanced Recovery After Surgery (ERAS) protocol.
In outpatient surgery, postoperative pain management requires new strategies and/or organizational approaches to ensure high-quality pain management from the very start.
The principle of analgesia for acute postoperative pain recommends: i) routine, fixed-schedule maintenance therapy; and ii) rescue therapy if maintenance therapy is insufficient, based on pain titration, using mild or strong oral opioids.
Postoperative pain is the primary focus of postoperative care but the goal is also to improve postoperative recovery and enhance the patient's overall care.
To date, there are no medical telemonitoring devices to support the patient in properly taking their analgesics based on multiple-daily assessments of the efficacy and tolerability of the analgesic treatment, enabling systematic postoperative screening for early and late warning signs of the risk of chronic pain.
The Thess Monitoring device, which implements the ANTALGEEK® protocol, (TMA) was developed to optimize the efficiency of outpatient management of acute postoperative pain.
It improves patients' adherence to maintenance treatment with adaptive, personalized control of analgesia through better use of opioid rescue therapy, and the reduction of adverse effects associated with improper opioid use (under- or over-dosing).
The aim is to ensure optimal pain resolution and improve early and late postoperative recovery during the first postoperative week.
The TMA system enables remote monitoring of the efficacy and tolerability of analgesic treatment, as well as early and late warning signs of the risk of chronic pain.
By measuring pain scores daily during the first postoperative week, it identifies patients with a suboptimal pain trajectory who are at high risk of developing persistent pain beyond the third month.
It also assesses warning signs of the risk of chronic pain (neuropathic pain, persistent opioid use) at intervals following the procedure (Day 8, Month 1, Month 2, Month 3).
Improving the patient care pathway via the TMA system should make it possible to better coordinate postoperative follow-up between hospital-based and community-based care.
調査の概要
状態
募集
詳細な説明
The problem of acute postoperative pain (APOP) is a major public health problem, affecting nearly 10 million patients in France each year and potentially leading to numerous complications when inadequately managed. In the postoperative period, the implementation of effective analgesic therapy is a key factor in reducing early postoperative morbidity and mortality. Furthermore, poorly controlled PPS is one of the major risk factors for the development of chronic postoperative pain (CPOP). Optimizing analgesic medication to prevent an abnormal pain trajectory during the first postoperative week is a key strategy for preventing chronic postoperative pain.
Today, within the French healthcare system, an increasing number of patients undergo surgical procedures performed on an outpatient basis. The big challenge is to manage postoperative pain in the homes of patients who have undergone increasingly complex surgical procedures, either following outpatient surgery or after an early return home as part of an Enhanced Recovery After Surgery (ERAS) protocol.
In outpatient surgery, improving postoperative pain management requires the implementation of new strategies and/or organizational approaches to ensure a high-quality pain management pathway from the very beginning.
The principle of analgesia for acute postoperative pain recommends a combination of: i) routine, fixed-schedule maintenance therapy; and ii) rescue therapy-if maintenance therapy is insufficient-based on the principle of pain titration, using oral opioids (mild or strong). While postoperative pain remains the primary focus of postoperative care, the goal is also to improve postoperative recovery more broadly and thereby enhance the patient's overall care.
The assessment of postoperative recovery in outpatient surgery patients using a medical telemonitoring device is associated with a reduction in discomfort caused by various postoperative symptoms, including postoperative pain. However, to date, there is no medical telemonitoring device that both supports the patient in properly taking their analgesics based on multiple-daily assessments of the efficacy and tolerability of the analgesic treatment, and enables systematic postoperative screening for early and late warning signs of the risk of chronic pain.
To this end, the Thess Monitoring medical telemonitoring device (which implements the ANTALGEEK® protocol) (TMA) was developed. It is a tool for continuous therapeutic support and postoperative telemonitoring designed to optimize the efficiency of outpatient management of acute postoperative pain in patients by improving adherence to maintenance therapy, adaptive and personalized control of analgesia through better use of opioid rescue therapy, and the reduction of adverse effects associated with improper opioid use (under- or over-dosing), with the goal of ensuring optimal pain resolution and improved early and late postoperative recovery during the first postoperative week (Baseline-Day 7). To achieve this, the TMA system enables remote monitoring of the efficacy and tolerability of analgesic treatment, as well as early and late warning signs of the risk of chronic pain: identify, through daily measurement of pain scores during the first postoperative week, patients with a suboptimal pain trajectory who are at high risk of developing persistent postoperative pain beyond the third month; assess warning signs of the risk of chronic pain (neuropathic pain, persistent opioid use) at intervals following the procedure (Day 8, Month 1, Month 2, Month 3).
Improving the patient care pathway through the TMA system should thus make it possible to better coordinate postoperative follow-up between hospital-based and community-based care.
In this initial proof-of-concept study, the investigators aim to evaluate the performance and safety of the TMA medical device in the outpatient management of acute pain during the first postoperative week, as well as its impact on postoperative recovery and on reducing the risk of pain becoming chronic by the third postoperative month.
研究の種類
介入
入学 (推定)
150
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前：Anissa MEGZARI
- 電話番号：0466684236
- メール：drc@chu-nimes.fr
研究連絡先のバックアップ
- 名前：Joël LHERMITE, Dr.
- 電話番号：+334.66.68.30.50
- メール：joel.lhermite@chu-nimes.fr
研究場所
-
-
Gard
-
Nîmes、Gard、フランス、30029
- 募集
- Nîmes University Hospital
-
コンタクト：
- Anissa MEGZARI
- 電話番号：+33466684236
- メール：drc@chu-nimes.fr
-
コンタクト：
- Nimes U Hospital, Dr.
- 電話番号：+334.66.68.30.50
- メール：joel.lhermite@chu-nimes.fr
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
Inclusion Criteria:
- Patients eligible for outpatient surgery.
- Patients undergoing surgery likely to result in moderate to severe pain.
- Patients available for a 3-month follow-up.
- Patients who have provided their free and informed consent.
- Patients who have signed the consent form.
- Patients enrolled in or covered by a health insurance plan.
Exclusion Criteria:
- Patients participating in an interventional RIPH study involving a drug or classified as Category 1.
- Patients in an exclusion period determined by another study.
- Patients under judicial protection, guardianship, or conservatorship.
- Patients unable to express consent.
- Patient for whom it is impossible to provide informed information.
- Pregnant, laboring, or breastfeeding patients.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：支持療法
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
介入なし：Postoperative pain management : standard care
Patients receiving standard postoperative analgesic care
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実験的：Postoperative pain management using the Thess telemonitoring device
Patients being monitored with the Thess Monitoring medical telemonitoring device in conjunction with the ANTALGEEK® protocol
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The Thess monitoring medical device (Thess Corp., Montpellier) uses the remote ANTALGEEK® telemonitoring protocol to manage pain in outpatients who have had surgery causing moderate-to-severe pain.
It digitalizes and optimizes acute postoperative pain management at home by improving adherence to maintenance therapy, with adaptive, tailored control of analgesia through better use of opioid rescue therapy to reduce the adverse effects of opioid misuse and ensures optimal pain resolution and postoperative recovery during the first week.
The ANTALGEEK decision-making algorithm and a medical telemonitoring protocol help patients follow their pain medication regimen, monitoring them in postoperative Week 1, based on the preoperative prescription, data on the patient's adherence to treatment, its efficacy and tolerability.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Performance of the TMA® medical device (TMA group) according to the QoR-15 questionnaire score in the experimental group
時間枠：Day 2
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
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Day 2
|
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Performance of the TMA® medical device (TMA group) according to the QoR-15 questionnaire score in the standard care (control) group.
時間枠：Day 2
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
|
Day 2
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Quality of postoperative recovery (QoR15) during the early and late phases of recovery in the experimental group
時間枠：Day 1, before the intervention
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
|
Day 1, before the intervention
|
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Quality of postoperative recovery (QoR15) during the early and late phases of recovery in the experimental group
時間枠：Day 1, after the intervention
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
|
Day 1, after the intervention
|
|
Quality of postoperative recovery (QoR15) during the early and late phases of recovery in the experimental group
時間枠：Day 7
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
|
Day 7
|
|
Quality of postoperative recovery (QoR15) during the early and late phases of recovery in the standard care (control) group
時間枠：Day 1, before the intervention
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
|
Day 1, before the intervention
|
|
Quality of postoperative recovery (QoR15) during the early and late phases of recovery in the standard care (control) group
時間枠：Day 1, after the intervention
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
|
Day 1, after the intervention
|
|
Quality of postoperative recovery (QoR15) during the early and late phases of recovery in the standard care (control) group
時間枠：Day 7
|
The QoR-15 (quality of recovery) questionnaire comprises 15 items assessing different aspects of a patient's recovery : symptoms, functional status, and emotional well-being.
The 15 items are grouped into five domains: Physical Comfort (symptoms like nausea, vomiting, and general discomfort), Emotional State (feelings such as anxiety, depression, or general well-being), Physical Independence (the patient's ability to look after themselves, such as mobility and self-care), Psychological Support (feelings of support and reassurance) Pain (the level of pain experienced by the patient).
Each item in the QoR-15 is scored on an 11-point numerical scale ranging from 0 (none of the time/worst outcome) to 10 (all of the time/best outcome).
The sum of the scores for each of the 15 items results in a score ranging from 0 (very poor recovery) to 150 (excellent quality of recovery).
Excellent: QoR-15 score > 135, Good: QoR-15 score between 122 and 135 (inclusive), Moderate: QoR-15 score between 90
|
Day 7
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Pain progression in the experimental group
時間枠：Day 1
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Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Day 1
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Pain progression in the experimental group
時間枠：Day 2
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Day 2
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Pain progression in the experimental group
時間枠：Day 3
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Day 3
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Pain progression in the experimental group
時間枠：Day 4
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Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Day 4
|
|
Pain progression in the experimental group
時間枠：Day 5
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Day 5
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Pain progression in the experimental group
時間枠：Day 6
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Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Day 6
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Pain progression in the experimental group
時間枠：Day 7
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Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Day 7
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Pain progression in the experimental group
時間枠：Month 1
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Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Month 1
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Pain progression in the experimental group
時間枠：Month 2
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Month 2
|
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Pain progression in the experimental group
時間枠：Month 3
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Month 3
|
|
Pain progression in the in the standard care (control) group
時間枠：Day 1
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Day 1
|
|
Pain progression in the in the standard care (control) group
時間枠：Day 2
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Day 2
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Pain progression in the in the standard care (control) group
時間枠：Day 3
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Day 3
|
|
Pain progression in the in the standard care (control) group
時間枠：Day 4
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Day 4
|
|
Pain progression in the in the standard care (control) group
時間枠：Day 5
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Day 5
|
|
Pain progression in the in the standard care (control) group
時間枠：Day 6
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Day 6
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|
Pain progression in the in the standard care (control) group
時間枠：Day 7
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Day 7
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|
Pain progression in the in the standard care (control) group
時間枠：Month 1
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Month 1
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Pain progression in the in the standard care (control) group
時間枠：Month 2
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
|
Month 2
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Pain progression in the in the standard care (control) group
時間枠：Month 3
|
Average pain score over 24 hours according to the Visual Analog Scale (0 -10)
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Month 3
|
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Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Day 1
|
Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 1
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Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Day 1
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 1
|
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Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Day 2
|
Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 2
|
|
Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Day 2
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 2
|
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Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Day 3
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Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 3
|
|
Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Day 3
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 3
|
|
Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Day 4
|
Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 4
|
|
Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Day 4
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 4
|
|
Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Day 5
|
Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 5
|
|
Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Day 5
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 5
|
|
Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Day 6
|
Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 6
|
|
Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Day 6
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 6
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Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Day 7
|
Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 7
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|
Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Day 7
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Day 7
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Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Day 1
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Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection via the Tess Monitoring Application
|
Day 1
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Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Day 1
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Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical registration form
|
Day 1
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|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Day 2
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Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection via the Tess Monitoring Application
|
Day 2
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Day 2
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical monitoring form
|
Day 2
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Day 3
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection via the Tess Monitoring Application
|
Day 3
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Day 3
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical registration form
|
Day 3
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Day 4
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up. Data collection via the Tess Monitoring Application |
Day 4
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Day 4
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical registration form
|
Day 4
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Day 5
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up. Data collection via the Tess Monitoring Application |
Day 5
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Day 5
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical registration form
|
Day 5
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Day 6
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection via the Tess Monitoring Application
|
Day 6
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Day 6
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical registration form
|
Day 6
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Day 7
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection via the Tess Monitoring Application
|
Day 7
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Day 7
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical monitoring form
|
Day 7
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Month 1
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection via the Tess Monitoring Application and a phone call to the patient
|
Month 1
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Month 1
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical registration form and a phone call to the patient
|
Month 1
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the experimental group
時間枠：Month 3
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection via the Tess Monitoring Application and a phone call to the patient
|
Month 3
|
|
Use of medication (including opioid medications and treatments outside the standard regimen) in the standard care (control) group
時間枠：Month 3
|
Collection of data on treatments prescribed outside the standard regimen and prescriptions issued on discharge from hospital up to three months of follow-up.
Data collection on the electronic clinical registration form and a phone call to the patient
|
Month 3
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the experimental group
時間枠：Day 1
|
Data collection via the Tess Monitoring Application
|
Day 1
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the standard care (control) group
時間枠：Day 1
|
Data collection on the electronic clinical registration form
|
Day 1
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the experimental group
時間枠：Day 2
|
Data collection via the Tess Monitoring Application
|
Day 2
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the standard care (control) group
時間枠：Day 2
|
Data collection on the electronic clinical registration form
|
Day 2
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the experimental group
時間枠：Day 3
|
Data collection via the Tess Monitoring Application
|
Day 3
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the standard care (control) group
時間枠：Day 3
|
Data collection on the electronic clinical registration form
|
Day 3
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the experimental group
時間枠：Day 4
|
Data collection via the Tess Monitoring Application
|
Day 4
|
|
Number of unplanned medical appointments and telephone contacts with healthcare professionals after discharge from hospital in the standard care (control) group
時間枠：Day 4
|
Data collection on the electronic clinical registration form
|
Day 4
|
|
Prescription issued outside of those prescribed upon hospital discharge in the experimental group
時間枠：Month 3
|
Quantitative
|
Month 3
|
|
Prescription issued outside of those prescribed upon hospital discharge in the standard care(control) group
時間枠：Month 3
|
Quantitative
|
Month 3
|
|
Number of days of sick leave prescribed in the experimental group
時間枠：Month 3
|
Quantitative
|
Month 3
|
|
Number of days of sick leave prescribed in the standard care (control) group
時間枠：Month 3
|
Quantitative
|
Month 3
|
|
Satisfaction questionnaire administered to the patient in the experimental group
時間枠：Day 3
|
Qualitative
|
Day 3
|
|
Satisfaction questionnaire administered to the patient in the standard care (control) group
時間枠：Day 3
|
Qualitative
|
Day 3
|
|
Satisfaction questionnaire administered to the anesthesiologist in the experimental group
時間枠：End of the inclusion period
|
Qualitative
|
End of the inclusion period
|
|
Satisfaction questionnaire administered to the anesthesiologist in the standard care (control) group
時間枠：End of the inclusion period
|
Qualitative
|
End of the inclusion period
|
|
System Usability Scale score during the follow-up call to patients in the experimental group
時間枠：Day 30
|
The System Usability Scale (SUS) score is a measure of the usability of an interactive system, derived from a questionnaire that includes ten items.
Each item is presented as a positive statement, and users are asked to indicate their agreement or disagreement with it using a 5-point Likert scale.
The score is recalculated based on the number of items answered correctly, with a score of 2.5 for each item.
This scoring system allows the assessment of user satisfaction and the overall usability of the system.
|
Day 30
|
|
System Usability Scale score from health providers to the experimental group
時間枠：End of the inclusion period
|
The System Usability Scale (SUS) score is a measure of the usability of an interactive system, derived from a questionnaire that includes ten items.
Each item is presented as a positive statement, and users are asked to indicate their agreement or disagreement with it using a 5-point Likert scale.
The score is recalculated based on the number of items answered correctly, with a score of 2.5 for each item.
This scoring system allows the assessment of user satisfaction and the overall usability of the system.
|
End of the inclusion period
|
|
System Usability Scale score during the follow-up call to patients in the standard care (control) group
時間枠：Day 30
|
The System Usability Scale (SUS) score is a measure of the usability of an interactive system, derived from a questionnaire that includes ten items.
Each item is presented as a positive statement, and users are asked to indicate their agreement or disagreement with it using a 5-point Likert scale.
The score is recalculated based on the number of items answered correctly, with a score of 2.5 for each item.
This scoring system allows the assessment of user satisfaction and the overall usability of the system.
|
Day 30
|
|
System Usability Scale score from health providers to the standard care (control) group
時間枠：End of the inclusion period
|
The System Usability Scale (SUS) score is a measure of the usability of an interactive system, derived from a questionnaire that includes ten items.
Each item is presented as a positive statement, and users are asked to indicate their agreement or disagreement with it using a 5-point Likert scale.
The score is recalculated based on the number of items answered correctly, with a score of 2.5 for each item.
This scoring system allows the assessment of user satisfaction and the overall usability of the system.
|
End of the inclusion period
|
|
DN2 questionnaire score in the experimental group
時間枠：Post-operative Month 1
|
The DN2 questionnaire is a simplified version of the DN4 (omitting the clinical examination), developed in France in 2005 by Bouhassira and the French Neuropathic Pain Group.
It consists of two questions assessing the presence or absence of seven symptoms suggestive of neuropathic pain : burning, painful cold, electric shocks, tingling, prickling, numbness, and itching.
The cutoff for a positive DN2 result is set at 3 out of 7 points.
A positive DN2 result does not establish a formal diagnosis of neuropathic pain, as a clinical examination remains essential.
|
Post-operative Month 1
|
|
DN2 questionnaire score in the experimental group
時間枠：Post-operative Month 2
|
The DN2 questionnaire is a simplified version of the DN4 (omitting the clinical examination), developed in France in 2005 by Bouhassira and the French Neuropathic Pain Group.
It consists of two questions assessing the presence or absence of seven symptoms suggestive of neuropathic pain : burning, painful cold, electric shocks, tingling, prickling, numbness, and itching.
The cutoff for a positive DN2 result is set at 3 out of 7 points.
A positive DN2 result does not establish a formal diagnosis of neuropathic pain, as a clinical examination remains essential.
|
Post-operative Month 2
|
|
DN2 questionnaire score in the experimental group
時間枠：Post-operative Month 3
|
The DN2 questionnaire is a simplified version of the DN4 (omitting the clinical examination), developed in France in 2005 by Bouhassira and the French Neuropathic Pain Group.
It consists of two questions assessing the presence or absence of seven symptoms suggestive of neuropathic pain : burning, painful cold, electric shocks, tingling, prickling, numbness, and itching.
The cutoff for a positive DN2 result is set at 3 out of 7 points.
A positive DN2 result does not establish a formal diagnosis of neuropathic pain, as a clinical examination remains essential.
|
Post-operative Month 3
|
|
DN2 questionnaire score in the standard care (control) group
時間枠：Post-operative Month 1
|
The DN2 questionnaire is a simplified version of the DN4 (omitting the clinical examination), developed in France in 2005 by Bouhassira and the French Neuropathic Pain Group.
It consists of two questions assessing the presence or absence of seven symptoms suggestive of neuropathic pain : burning, painful cold, electric shocks, tingling, prickling, numbness, and itching.
The cutoff for a positive DN2 result is set at 3 out of 7 points.
A positive DN2 result does not establish a formal diagnosis of neuropathic pain, as a clinical examination remains essential.
|
Post-operative Month 1
|
|
DN2 questionnaire score in the standard care (control) group
時間枠：Post-operative Month 2
|
The DN2 questionnaire is a simplified version of the DN4 (omitting the clinical examination), developed in France in 2005 by Bouhassira and the French Neuropathic Pain Group.
It consists of two questions assessing the presence or absence of seven symptoms suggestive of neuropathic pain : burning, painful cold, electric shocks, tingling, prickling, numbness, and itching.
The cutoff for a positive DN2 result is set at 3 out of 7 points.
A positive DN2 result does not establish a formal diagnosis of neuropathic pain, as a clinical examination remains essential.
|
Post-operative Month 2
|
|
DN2 questionnaire score in the standard care (control) group
時間枠：Post-operative Month 3
|
The DN2 questionnaire is a simplified version of the DN4 (omitting the clinical examination), developed in France in 2005 by Bouhassira and the French Neuropathic Pain Group.
It consists of two questions assessing the presence or absence of seven symptoms suggestive of neuropathic pain : burning, painful cold, electric shocks, tingling, prickling, numbness, and itching.
The cutoff for a positive DN2 result is set at 3 out of 7 points.
A positive DN2 result does not establish a formal diagnosis of neuropathic pain, as a clinical examination remains essential.
|
Post-operative Month 3
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the experimental group
時間枠：Baseline
|
Patient's declaration in the Thess Monitoring Application
|
Baseline
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the standard care (control) group
時間枠：Baseline
|
Phone call from the patient
|
Baseline
|
|
rate of adherence to the standard pain management regimen (non-opioid analgesics) in the in the standard care (control) group
時間枠：Day 1
|
Phone call from the patient
|
Day 1
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the experimental group
時間枠：Day 2
|
Patient's declaration in the Thess Monitoring Application
|
Day 2
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the standard care (control) group
時間枠：Day 2
|
Phone call from the patient
|
Day 2
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the experimental group
時間枠：Day 3
|
Patient's declaration in the Thess Monitoring Application
|
Day 3
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the standard care (control) group
時間枠：Day 3
|
Phone call from the patient
|
Day 3
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the experimental group
時間枠：Day 4
|
Patient's declaration in the Thess Monitoring Application
|
Day 4
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the standard care (control) group
時間枠：Day 4
|
Phone call from the patient
|
Day 4
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the experimental group
時間枠：Day 5
|
Patient's declaration in the Thess Monitoring Application
|
Day 5
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the standard care (control) group
時間枠：Day 5
|
Phone call from the patient
|
Day 5
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the experimental group
時間枠：Day 6
|
Patient's declaration in the Thess Monitoring Application
|
Day 6
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the standard care (control) group
時間枠：Day 6
|
Phone call from the patient
|
Day 6
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the experimental group
時間枠：Day 7
|
Patient's declaration in the Thess Monitoring Application
|
Day 7
|
|
Rate of adherence to the standard pain management regimen (non-opioid analgesics) in the standard care (control) group
時間枠：Day 7
|
Phone call from the patient
|
Day 7
|
|
Incidence of adverse effects associated with opioid use in the experimental group
時間枠：Baseline
|
Adverse effects associated with opioid use will be recorded on the Thess Monitoring Application Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Baseline
|
|
Incidence of adverse effects associated with opioid use in the standard care (control) group
時間枠：Baseline
|
Adverse effects associated with opioid use will be recorded via a phone call to the patient Nausea: yes/no Drowsiness: yes/no Dizziness: yes/no Itching: yes/no
|
Baseline
|
|
Adverse Events [Safety and Tolerability] in the experimental group
時間枠：Day 7
|
Qualitative assessment.
Any adverse events of any cause related to treatment will be recorded in the electronic clinical registration form following a phone call to the patient.
|
Day 7
|
|
Adverse Events [Safety and Tolerability]in the standard care (control) group
時間枠：Day 7
|
Qualitative assessment.
Any adverse events of any cause related to treatment will be recorded in the electronic clinical registration form following a phone call to the patient.
|
Day 7
|
|
Rate of incidents, malfunctions, and organization deviations that occurred during implementation in the experimental group
時間枠：Month 3
|
Qualitative
|
Month 3
|
|
Time spent connected to the Thess Monitoring device per patient in the experimental group
時間枠：Month 3
|
Quantitative, in minutes
|
Month 3
|
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研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2025年12月1日
一次修了 (推定)
2026年8月1日
研究の完了 (推定)
2026年12月31日
試験登録日
最初に提出
2026年6月26日
QC基準を満たした最初の提出物
2026年6月26日
最初の投稿 (実際)
2026年7月2日
学習記録の更新
投稿された最後の更新 (実際)
2026年7月8日
QC基準を満たした最後の更新が送信されました
2026年7月6日
最終確認日
2026年7月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。