- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07622355
Effects of Different Administration Routes of Dexmedetomidine on Postoperative Sleep Quality in Patients Undergoing Thyroidectomy
2026년 5월 27일 업데이트: Zhu Guoying, The Second People's Hospital of Huai'an
Effects of Different Perioperative Administration Routes of Dexmedetomidine on Postoperative Sleep Quality in Patients Undergoing Thyroidectomy: A Randomized Controlled Trial
Patients undergoing thyroid surgery often experience significant preoperative anxiety and show high concern about voice changes, scar formation and other related issues.
Postoperative neck discomfort and dysphagia also tend to disrupt normal sleep.
Dexmedetomidine activates α₂ receptors in the mesencephalic-pontine-medullary reticular formation, inhibits the release of norepinephrine, and induces a sleep state similar to non-rapid eye movement (NREM) sleep, particularly the N2 stage, which is closer to physiological sleep.
This study aimed to explore the effects of intranasal spray versus intravenous administration of dexmedetomidine on postoperative sleep quality in patients undergoing thyroidectomy.
By optimizing preoperative pharmacological intervention, it intends to improve patients' postoperative sleep quality, relieve pain and reduce postoperative adverse reactions, enhance recovery quality, and optimize patients' satisfaction and comfort level.
연구 개요
상태
모집하지 않고 적극적으로
정황
상세 설명
This randomized controlled trial was conducted to evaluate the effects of different administration routes of dexmedetomidine on postoperative sleep quality in patients undergoing thyroidectomy.
A total of 120 patients were randomized into three groups in a 1:1:1 ratio using computer-generated randomization and sealed opaque envelopes.IN-D group: Intranasal dexmedetomidine plus intravenous placebo.
Dexmedetomidine 1.0 μg/kg (maximum 100 μg) was administered intranasally via alternating nostrils 30 minutes before surgery, with an equal volume of 0.9% saline infused intravenously.IV-D group: Intravenous dexmedetomidine plus intranasal placebo.
A loading dose of dexmedetomidine 0.5 μg/kg was infused intravenously over 10 minutes 30 minutes preoperatively, with an equal volume of 0.9% saline administered intranasally.Control group: Intranasal and intravenous placebo (0.9% saline in both routes).Patients, attending anesthesiologists, and outcome assessors were blinded to group allocation throughout the study.
Intraoperative anesthesia management was performed by a separate anesthesiologist not involved in data assessment to maintain blinding.
All patients fasted for 6 hours and restricted clear fluids for 2 hours preoperatively.
No premedication was administered.Upon arrival in the operating room, standard monitoring was applied, including electrocardiography (ECG), pulse oximetry (SpO₂), and non-invasive blood pressure (NIBP).
Invasive arterial cannulation was performed for continuous blood pressure monitoring.General anesthesia was induced with etomidate 0.2 mg/kg, rocuronium 0.6 mg/kg, sufentanil 0.5 μg/kg, and propofol 1.5 mg/kg.
After 5 minutes of preoxygenation, tracheal intubation was performed under video laryngoscopy.
Mechanical ventilation was initiated with pure oxygen at 2.0 L/min, with tidal volume 6-8 mL/kg, I:E ratio 1:2, and PETCO₂ maintained at 35-45 mmHg.
Correct positioning of the neuromonitoring endotracheal tube was verified after intubation.Anesthesia depth was maintained at an entropy index (RE/SE) of 40-60 by adjusting infusions of propofol and remifentanil and the concentration of sevoflurane.
Hemodynamic stability was maintained using vasoactive agents (ephedrine, phenylephrine, nitroglycerin) as needed.All anesthetics were stopped at skin closure.
Patients were transferred to the post-anesthesia care unit (PACU) immediately after surgery.
Tracheal extubation was performed when patients recovered consciousness and adequate spontaneous respiration.
연구 유형
중재적
등록 (실제)
120
단계
- 2 단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
-
-
-
Huai'an, 중국
- The Affiliated Huaian Hospital of Xuzhou Medical University, Huai'an Second Hospital, Huaian
-
-
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
아니
설명
Inclusion Criteria:
- Age: 18-65 years old
- ASA classification: Grade I or II
- BMI: 18-30 kg/m²
- Planned to undergo thyroid benign tumor or thyroid malignant tumor resection under general anesthesia
- No history of sedatives or sleeping pills used within 1 week before surgery
- Agree to participate in the study and sign the informed consent form
Exclusion Criteria:
- History of sleep disorders or mental illness
- Use of sleep-affecting drugs such as antidepressants and sleeping pills
- Allergy to dexmedetomidine and other drugs
- Patients with nasal lesions or intolerance to nasal sprays
- Cardiac conduction block, severe bradycardia or hypotension
- Pregnant or lactating women
- Patients with severe dysfunction of the heart, brain, lungs, liver, kidneys or other organs
- Patients with difficult airway during anesthesia induction who need to change the conventional intubation method
- Patients who refuse to participate in this study and do not sign the informed consent form
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 삼루타
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Dexmedetomidine Nasal Spray Group
Thirty minutes before surgery, 1.0 μg/kg of dexmedetomidine nasal spray (adult dosage, maximum dose not exceeding 100 μg) is administered by alternating bilateral nasal inhalation.
Meanwhile, an equal volume of 0.9% normal saline is infused via intravenous pump.
|
Thirty minutes before surgery, 1.0 μg/kg of dexmedetomidine nasal spray (adult dosage, maximum dose not exceeding 100 μg) is administered by alternating bilateral nasal inhalation.
Meanwhile, an equal volume of 0.9% normal saline is infused via intravenous pump.
Thirty minutes before surgery, dexmedetomidine 0.5 μg/kg is administered intravenously as a 10-minute loading dose, with an equal volume of 0.9% normal saline given via nasal spray simultaneously.
|
|
실험적: Dexmedetomidine Intravenous Group
Thirty minutes before surgery, dexmedetomidine 0.5 μg/kg is administered intravenously as a 10-minute loading dose, with an equal volume of 0.9% normal saline given via nasal spray simultaneously.
|
Thirty minutes before surgery, 1.0 μg/kg of dexmedetomidine nasal spray (adult dosage, maximum dose not exceeding 100 μg) is administered by alternating bilateral nasal inhalation.
Meanwhile, an equal volume of 0.9% normal saline is infused via intravenous pump.
Thirty minutes before surgery, dexmedetomidine 0.5 μg/kg is administered intravenously as a 10-minute loading dose, with an equal volume of 0.9% normal saline given via nasal spray simultaneously.
|
|
위약 비교기: Control Group
An equal volume of 0.9% normal saline is administered via both nasal spray and intravenous route.
|
An equal volume of 0.9% normal saline is administered via both nasal spray and intravenous route.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Richards-Campbell Sleep Questionnaire(RCSQ)
기간: Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
This scale was developed by Richards et al.
It is a simple self-report scale specifically designed for ICU patients, widely used in sleep assessment research in critical care medicine and post-anesthesia fields.
The RCSQ includes 6 items: the first 5 are core scoring items, assessing sleep depth, difficulty in falling asleep, number of awakenings, ability to fall back asleep, and overall sleep quality respectively; the 6th is an environmental noise assessment item (not included in the total score, only for reference).
Each core item uses a 100 mm Visual Analog Scale (VAS): the left end is 0 points (worst state), the right end is 100 points (best state), and the score is the distance from the left end to the subject's marked position.
The total score is the arithmetic mean of the 5 core items (range 0-100 points), with higher scores indicating better sleep.
Clinical grading: <50 points (poor), 50-69 points (moderate), ≥70 points (good).
|
Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Pittsburgh Sleep Quality Index(PSQI)
기간: Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
The Pittsburgh Sleep Quality Index (PSQI) is a self-reported questionnaire used to assess sleep quality and sleep disorders.
It consists of 19 self-reported questions and is used to calculate seven dimensions of sleep: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep-inducing drugs, and daytime functional impairment.
Each component is scored on a 0-3 scale, and the total score is the sum of the seven dimensions (ranging from 0 to 21 points).
A total score greater than 5 points indicates the presence of sleep disorders, and the higher the score, the worse the sleep quality.
|
Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
|
The sleep data recorded by the Fitbit Charge 6 bracelet
기간: Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
The sleep data recorded by the Fitbit Charge 6 bracelet includes sleep timeline, awake time, rapid eye movement (REM) sleep, light sleep, deep sleep, and sleep score.
|
Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
|
Visual Analog Scale(VAS)
기간: 6 Hours Post-Operative, 12 Hours Post-Operative, 24 Hours Post-Operative, 48 Hours Post-Operative
|
The Visual Analog Scale (VAS) is a tool used to assess the intensity of subjective symptoms (such as pain, itching, anxiety, etc.).
Through a line of fixed length (usually 10 cm), patients mark the severity of their current symptoms based on their own feelings.
The scale is a horizontal straight line, with "no symptoms" (0 points) marked at one end and "the most severe symptoms" (10 points) at the other end.
Patients mark a position on the line that matches their symptoms, and the rater measures the distance from the starting point to the marked position, which is converted into a score ranging from 0 to 10 points.
A score of 0 means no symptoms at all (e.g., no pain), 1-3 points indicate mild symptoms (not affecting daily life), 4-6 points indicate moderate symptoms (affecting life but tolerable), and 7-10 points indicate severe symptoms (intolerable and requiring urgent intervention).
|
6 Hours Post-Operative, 12 Hours Post-Operative, 24 Hours Post-Operative, 48 Hours Post-Operative
|
|
Richmond Agitation and Sedation Scale(RASS)
기간: 6 Hours Post-Operative, 12 Hours Post-Operative, 24 Hours Post-Operative, 48 Hours Post-Operative
|
The Richmond Agitation-Sedation Scale (RASS) is a widely used tool to assess the level of sedation and agitation in patients.
It ranges from +4 to -5, with specific descriptors for each score: +4 indicates combative behavior; +3 is extremely agitated; +2 means agitated and restless ; +1 denotes restless but calm; 0 represents alert and calm; -1 is drowsy; -2 indicates light sedation; -3 means moderate sedation; -4 is deep sedation ; and -5 represents unarousable.
This scale helps clinicians objectively evaluate and adjust sedation levels to ensure patient comfort and safety.
|
6 Hours Post-Operative, 12 Hours Post-Operative, 24 Hours Post-Operative, 48 Hours Post-Operative
|
|
The Quality of Recovery-15(QoR-15)
기간: Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
The QoR-15 scale is divided into five dimensions: physical comfort (5 items), self-care (2 items), psychological support (2 items), emotional state (4 items), and pain (2 items), with each item rated on a scale of 0-10, and the total score ranging from 0-150, with the higher the score the better the quality of recovery, and a score of 118 and above indicating surgery.
|
Preoperative day 1,Postoperative day 0,Postoperative day 1,Postoperative day 7,Pre-discharge
|
|
Drug use
기간: Perioperative
|
Record the intraoperative consumption of propofol and remifentanil, the names and dosages of intraoperative vasoactive drugs, and the postoperative consumption of rescue analgesics (including PACU).
|
Perioperative
|
|
Hemodynamic indicators
기간: Baseline,Pre-Intervention ,Before Intubation,Immediately After Intubation,5 Minutes After Intubation,At the Time of Skin Incision,30 Minutes After the Start of Surgery,At the End of Surgery,Before Extubation,At PACU Discharge
|
The perioperative blood pressure, heart rate (HR) and mean arterial pressure (MAP) are important hemodynamic indicators for evaluating the patient's perioperative condition.
|
Baseline,Pre-Intervention ,Before Intubation,Immediately After Intubation,5 Minutes After Intubation,At the Time of Skin Incision,30 Minutes After the Start of Surgery,At the End of Surgery,Before Extubation,At PACU Discharge
|
|
Time
기간: Perioperative
|
Record the duration of surgery, awakening time (the time from the cessation of anesthetics to the patient's spontaneous eye opening), extubation time (the time from the cessation of anesthetics to the patient's extubation), time of discharge from the PACU, and postoperative hospital stay.
|
Perioperative
|
|
Adverse Reaction
기간: Perioperatively and Through 48 Hours After Surgery
|
Record adverse reactions such as hypotension, bradycardia, nausea and vomiting, dizziness, sore throat, hoarseness, respiratory depression, bleeding, postoperative pain, dysphagia, tremor, facial nerve sign, Trousseau's sign, dry mouth, and dry nose.
|
Perioperatively and Through 48 Hours After Surgery
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
수사관
- 수석 연구원: Jun Wang, The Second People's Hospital of Huai'an
간행물 및 유용한 링크
연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.
일반 간행물
- He J, Zhang X, Li C, Fu B, Huang Y, Li H. Dexmedetomidine nasal administration improves perioperative sleep quality and neurocognitive deficits in elderly patients undergoing general anesthesia. BMC Anesthesiol. 2024 Jan 30;24(1):42. doi: 10.1186/s12871-024-02417-9.
- Liu H, Wei H, Qian S, Liu J, Xu W, Luo X, Fang J, Liu Q, Cai F. Effects of dexmedetomidine on postoperative sleep quality: a systematic review and meta-analysis of randomized controlled trials. BMC Anesthesiol. 2023 Mar 21;23(1):88. doi: 10.1186/s12871-023-02048-6.
- Wang L, Liang XQ, Sun YX, Hua Z, Wang DX. Effect of perioperative dexmedetomidine on sleep quality in adult patients after noncardiac surgery: A systematic review and meta-analysis of randomized trials. PLoS One. 2024 Dec 5;19(12):e0314814. doi: 10.1371/journal.pone.0314814. eCollection 2024.
- Wu J, Liu X, Ye C, Hu J, Ma D, Wang E. Intranasal dexmedetomidine improves postoperative sleep quality in older patients with chronic insomnia: a randomized double-blind controlled trial. Front Pharmacol. 2023 Nov 16;14:1223746. doi: 10.3389/fphar.2023.1223746. eCollection 2023.
- Maras Baydogan G, Surme Y, Kutuk Karasungur S. The challenges experienced by patients in the early period after thyroidectomy and the effects on sleep quality. Support Care Cancer. 2025 May 1;33(5):438. doi: 10.1007/s00520-025-09483-w.
- Koo DL, Park Y, Nam H, Chai YJ. Sleep quality of patients with papillary thyroid carcinoma: a prospective longitudinal study with 5-year follow-up. Sci Rep. 2022 Nov 5;12(1):18823. doi: 10.1038/s41598-022-23549-3.
- Wang Y, Jin Z, Xu W, Chen K, Wei L, Yang D, Deng X, Tong S. Clinical observation of dexmedetomidine nasal spray in the treatment of sleep disorders on the first night after undergoing maxillofacial surgery: a single-center double-blind randomized controlled study. J Pharm Pharm Sci. 2023 Oct 3;26:11699. doi: 10.3389/jpps.2023.11699. eCollection 2023.
- Li X, Yan L, Wang L, Chen H, Yang B. Study on the preventive effect of dexmedetomidine on anesthetic associated sleep disturbance in young to middle-aged female patients undergoing hysteroscopy: a study protocol for a crossover randomized controlled trial. Trials. 2024 Jul 15;25(1):480. doi: 10.1186/s13063-024-08311-6.
- Yang WY, Huang K, Lin ZJ, Zeng W, Liu X, Liu HB, Zhong ML, Wei J, Liang WD, Wang LF, Chen L. Intranasal Dexmedetomidine for the Management of Preoperative Anxiety-Related Insomnia: A Randomized, Three-Blinded, Clinical Trial Compared with Lorazepam and Placebo. Drug Des Devel Ther. 2024 Dec 17;18:6061-6073. doi: 10.2147/DDDT.S487463. eCollection 2024.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
2025년 9월 1일
기본 완료 (추정된)
2026년 6월 30일
연구 완료 (추정된)
2026년 7월 31일
연구 등록 날짜
최초 제출
2026년 5월 13일
QC 기준을 충족하는 최초 제출
2026년 5월 27일
처음 게시됨 (실제)
2026년 6월 3일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 6월 3일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 5월 27일
마지막으로 확인됨
2026년 5월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
갑상선 질환에 대한 임상 시험
-
University of Pennsylvania완전한Intrntl Classification of Diseases, 9th Revision, (ICD-9-CM) 410의 주진단 또는 이차진단 코드가 있는 환자(5번째 숫자가 2인 경우 제외)미국
Dexmedetomidine (DEX)에 대한 임상 시험
-
Molecular Partners AG완전한
-
King Faisal Specialist Hospital & Research Center완전한
-
Cliniques universitaires Saint-Luc- Université...아직 모집하지 않음심장 결함, 선천성
-
Sichuan Academy of Medical Sciences아직 모집하지 않음부패 | 패혈성 쇼크