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LINQ® Procedure vs. Conventional Medical Management for Sacroiliac Dysfunction (LINQT)

2026年7月21日 更新者:PainTEQ, LLC

LINQT: An Open Label Randomized, Controlled, Multicenter, Prospective, Long Term Clinical Study on the Minimally Invasive Posterior Sacroiliac Fusion Device LINQ® System

The objective of this clinical evaluation is to assess the safety and effectiveness of LINQ fusion procedure for treatment of sacroiliac joint (SIJ) dysfunction compared to Conservative Medical Management (CMM).

調査の概要

詳細な説明

Prospective, multi-center, open-label, randomized, clinical study. Subjects who meet the eligibility criteria and are enrolled will be randomized 2:1 to LINQ or CMM. After their 6 Month evaluations are complete, subjects in the Control Group can elect to stay in the CMM Arm or crossover to receive the LINQ procedure.

Each subject will undergo a Screening Visit, Randomization, Baseline Procedure or CMM Initiation Visit, and Follow-Up Visits through 24 Months. The primary endpoint is evaluated at the 6 Month Follow Up Visit.

Subjects that elect to crossover from the Control Group to the Treatment Group at the 6 Month Visit, will have Procedure and Follow-Up Visits through 18 Months post crossover procedure.

研究の種類

介入

入学 (推定)

200

段階

  • フェーズ 4

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

研究場所

    • Texas
      • Shenandoah、Texas、アメリカ、77384
        • 募集
        • Procura Pain and Spine
        • コンタクト:

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:

  • To be eligible to participate in this study, a subject must meet ALL of the following criteria, as determined by the Investigator:

    1. Age and Body Mass Index (BMI)

      1. Adult subjects aged ≥ 21 years at screening.
      2. BMI ≤ 40.
    2. Chronic SIJ-Related Pain

      1. Has experienced low back and/or buttock pain for at least 6 months that has been inadequately responsive to non-surgical management.
      2. Has experienced nonradicular pain that is maximal below the L5 vertebrae, localized over the posterior SIJ, and consistent with SIJ pain.
    3. Diagnosis of SIJ Dysfunction

      a. Has a diagnosis of SIJ dysfunction (degenerative sacroiliitis or SIJ disruption) based on ALL of the following: i. A positive Fortin's finger test; and ii. Pain elicited at least three (3) of five (5) SIJ-specific physical examination maneuvers (FABER test, Gaenslen's test, Distraction, Thigh Thrust, Compression); and iii. At least 75% reduction in pain, with associated improvement in previously painful maneuvers, for the expected duration of action following two (2) image-guided, contrast-enhanced intra-articular diagnostic SIJ injections, performed on separate visits using anesthetics with different durations of action; and iv. Completion of at least one (1) therapeutic intra-articular SIJ injection (e.g., corticosteroid injection) within the past 12 months.

    4. Baseline Disability and Pain Severity

      a. Baseline Oswestry Disability Index (ODI) score ≥30%; and b. Baseline SI joint pain score of ≥60 mm on a 100 mm Visual Analog Scale (VAS).

    5. Nicotine Abstinence

      a. Is able and willing to completely avoid all forms of nicotine (including smoking, vaping, e-cigarettes, tobacco, or nicotine pouches) for the entire duration of the study.

    6. Treatment Decision

      a. The treating physician has independently determined that the LINQ procedure is an appropriate treatment option for the subject's SIJ dysfunction in the course of routine clinical care, and the subject has agreed to undergo this treatment.

    7. Informed Consent and Compliance

      1. Is willing and capable of providing written informed consent; and
      2. Is willing and able to comply with all study-related requirements, procedures, and follow-up visits.

Exclusion Criteria:

  • Exclusion Criteria Subjects must meet none of the following criteria to be eligible for participation in this study, as determined by the Investigator:

    1. Pain Source Uncertainty a. Inability to confirm, in the Investigator's clinical judgment, that the subject's primary pain generator is the sacroiliac joint.
    2. Alternative Primary Spine Pathology

      a. Presence of severe low back pain attributable to other spinal pathology, including but not limited to lumbar disc degeneration, lumbar disc herniation, lumbar spondylolisthesis, lumbar spinal stenosis, lumbar facet degeneration, or lumbar vertebral body fracture.

    3. Other Sacroiliac Pathology

      a. Presence of known sacroiliac joint pathology other than degenerative SIJ dysfunction, including inflammatory sacroiliitis (e.g., ankylosing spondylitis or other HLA-associated spondyloarthropathies), tumor, infection, acute fracture, or crystal arthropathy.

    4. Non-SIJ Pain Syndromes

      a. History of coccydynia or prior coccygectomy, endometriosis, cluneal neuralgia, or pudendal neuralgia.

    5. Recent Sacral Interventions

      a. Prior sacral radiofrequency ablation performed within 6 months prior to enrollment.

    6. Recent Pelvic Trauma

      a. History of major pelvic trauma within 12 months prior to enrollment.

    7. Severe Osteoporosis

      a. Prior diagnosis or suspicion of severe osteoporosis, defined as a prior bone mineral density T-score of < -2.5 or a history of osteoporotic fracture.

    8. Medications Detrimental to Bone or Soft-Tissue Healing

      a. Current use of medications known to adversely affect bone quality or soft-tissue healing, as determined by the Investigator.

    9. Anatomic Constraints

      a. Anatomic anomalies or defects that, in the Investigator's opinion, would preclude safe or biomechanically appropriate device placement.

    10. Systemic Inflammatory or Rheumatologic Disease

      a. Presence of a chronic inflammatory rheumatologic condition, such as rheumatoid arthritis.

    11. Centralized Pain Syndromes

      a. Current diagnosis of fibromyalgia.

    12. Infection Risk

      a. Evidence of current local or systemic infection that would increase surgical risk.

    13. High-Dose Opioid Therapy (≥90 MME/day)

      a. Current use of systemic opioid analgesics at Screening/Baseline with an average daily dose ≥90 morphine milligram equivalents (MME/day), based on medication reconciliation (prescription records and subject report) and standard MME conversion factors.

    14. Current Nicotine Use (Self-Reported)

      a. Self-reported use of any nicotine-containing products (including smoking, vaping/e-cigarettes, cigars, pipes, smokeless tobacco, nicotine pouches, and nicotine replacement products) within 6 weeks prior to Screening/Baseline.

    15. Secondary Gain or Litigation

      a. Currently receiving or actively seeking workers' compensation or disability benefits or involved in injury-related litigation.

    16. Pregnancy

      a. Currently pregnant or planning to become pregnant within two (2) years following enrollment, as self-reported.

    17. Vulnerable Populations

      a. Individuals who are prisoners or wards of the state.

    18. Substance Abuse

      a. Known or suspected active drug or alcohol abuse, including opioid misuse.

    19. Psychiatric Conditions

      a. Diagnosed psychiatric disorder (e.g., schizophrenia, major depressive disorder, personality disorder) that, in the Investigator's judgment, could interfere with study participation.

    20. Concurrent Interventional Research

      a. Current participation in another clinical trial.

    21. Neurologic Conditions Affecting Rehabilitation

      a. Presence of a significant neurologic disorder that would interfere with participation in physical therapy or post procedural rehabilitation.

    22. Other Confounding Medical Conditions a. Any other medical condition or pain condition not intended to be treated in this study that, in the Investigator's judgment, could interfere with study procedures, accurate pain reporting, or interpretation of study endpoints.

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:処理
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • 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
アクティブコンパレータ:Treatment Arm (LINQ Procedure)
Subjects randomized to the Treatment Arm will undergo the LINQ Procedure.
The LINQ system is intended for use in patients with SIJ disease by implantation of compatible implants to prepare the SIJ for allograft fusion.
アクティブコンパレータ:Conventional Medical Management (CMM)
Subjects randomized to the CMM Control Arm shall receive standardized, stepwise, non-surgical management for SIJ pain.
CMM Control Arm shall receive standardized, stepwise, non-surgical management for SIJ pain.
他の名前:
  • Non-Surgical Management

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
Composite Success Responder Rate at Month 6
時間枠:Month 6

Unit of Measure: Percentage of participants

Description: The primary endpoint is a single binary (Yes/No) composite responder classification per subject at Month 6. A subject is classified as a composite success responder ONLY if ALL three of the following criteria are met:

Pain Improvement: Reduction in SIJ pain VAS score of ≥20 mm from baseline to Month 6 (VAS measured on 0-100 mm scale).

Safety: Absence of any device-related or procedure-related SAEs through Month 6 (Day 180).

Surgical Reintervention: No surgical reintervention for SIJ fusion through Month 6 (Day 180), including device removal (complete or partial), device revision or replacement, or reoperation at the index SIJ.

Subjects meeting all three components are classified as responders; the outcome is reported as the percentage (%) of participants classified as responders.

Month 6

二次結果の測定

結果測定
メジャーの説明
時間枠
Visual Analog Scale (VAS)
時間枠:Months 1, 3, 6, 12, 18, 24.
The Visual Analog Scale (VAS) is a patient-reported measure of pain intensity assessed using a 100 mm horizontal line anchored by 0 mm ("no pain") and 100 mm ("worst imaginable pain"). Scores range from 0 to 100 mm, with higher scores indicating greater pain severity. Change from baseline in VAS score and proportion of participants achieving a minimum clinically important difference (MCID) in pain intensity will be assessed. MCID is defined as a reduction of ≥20 mm from baseline on the 0-100 mm scale. Higher proportions indicate greater clinical improvement.
Months 1, 3, 6, 12, 18, 24.
Oswestry Disability Index (ODI)
時間枠:Months 1, 3, 6, 12, 18, 24
The Oswestry Disability Index (ODI) is a validated patient-reported questionnaire assessing disability related to low back pain across 10 domains of daily living. Scores range from 0 to 100, with higher scores indicating greater disability. Change from baseline in ODI score and proportion of participants achieving a minimum clinically important difference (MCID) in disability will be assessed using the Oswestry Disability Index (ODI). MCID is defined as a reduction of ≥15 points from baseline on the 0-100 scale. Higher proportions indicate greater clinical improvement.
Months 1, 3, 6, 12, 18, 24
Patient-Reported Outcomes Measurement Information System (PROMIS-29+2)
時間枠:Months 1, 3, 6, 12, 18, 24
The Patient-Reported Outcomes Measurement Information System 29-Item Profile v2.1 + 2 (PROMIS-29+2) assesses multiple health domains including physical function, anxiety, depression, fatigue, sleep disturbance, ability to participate in social roles, pain interference, and cognitive function. Domain scores are reported as T-scores standardized to a mean of 50 and standard deviation of 10 in the general population, with a typical range of approximately 20 to 80. Higher scores indicate more of the domain being measured (e.g., worse symptoms for anxiety, depression, fatigue, sleep disturbance, pain interference, and cognitive concerns; and better functioning for physical function and social participation). Change from baseline in T-scores will be evaluated.
Months 1, 3, 6, 12, 18, 24
EuroQol 5-Dimension 5-Level (EQ-5D-5L) questionnaire
時間枠:Months 1, 3, 6, 12, 18, 24
The EuroQol 5-Dimension 5-Level (EQ-5D-5L) questionnaire is a standardized measure of health-related quality of life assessing five domains: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Responses are converted into a single index score using country-specific value sets. The index score typically ranges from less than 0 (health states worse than death) to 1 (perfect health), where higher scores indicate better health status. Change from baseline in EQ-5D-5L index scores will be evaluated.
Months 1, 3, 6, 12, 18, 24
Patient Global Impression of Change (PGIC)
時間枠:Months 1, 3, 6, 12, 18, 24
The Patient Global Impression of Change (PGIC) is a patient-reported measure assessing overall change in health status since the start of treatment. It is a 7-point ordinal scale with responses ranging from 1 ("very much improved") to 7 ("very much worse"). Lower scores indicate greater improvement, and higher scores indicate worsening. The distribution of PGIC responses across categories will be summarized.
Months 1, 3, 6, 12, 18, 24
Medication use
時間枠:Months 1, 3, 6, 12, 18, 24
Medication use will be assessed at each visit, including opioid and non-opioid pain medications. Opioid consumption will be quantified as daily morphine milligram equivalents (MME), calculated using standard conversion factors. MME values range from 0 upward, with higher values indicating greater opioid use. Change from baseline in daily MME will be evaluated. Additional analyses may include the proportion of participants reducing or discontinuing opioid use over time.
Months 1, 3, 6, 12, 18, 24
Proportion of Participants Achieving Both a ≥20 mm Reduction in SIJ Pain VAS and a ≥15 Point Reduction in ODI
時間枠:Months 1, 3, 6, 12, 18, 24

Composite responder analysis based on two validated patient-reported outcomes. Pain intensity is measured using a 100 mm Visual Analog Scale (VAS) anchored by 0 mm ("no pain") and 100 mm ("worst imaginable pain"); higher scores indicate greater pain severity.

Disability is measured using the Oswestry Disability Index (ODI), a 10-item questionnaire assessing low back pain-related disability across domains of daily living, scored 0-100; higher scores indicate greater disability.

A participant is classified as a responder if they achieve BOTH a reduction of ≥20 mm from baseline in sacroiliac joint (SIJ) pain VAS AND a reduction of ≥15 points from baseline in ODI. The proportion of responders will be reported and a higher proportion indicates greater clinical improvement.

Months 1, 3, 6, 12, 18, 24
Incidence of Adverse Events
時間枠:Months 1, 3, 6, 12, 18, 24
Safety will be assessed by evaluating all adverse events (AEs) reported from the time of the index procedure through study completion. AEs will be characterized by severity, seriousness, and relatedness to the device and/or procedure. The number and proportion of participants experiencing one or more device- or procedure-related AEs and serious adverse events (SAEs) will be summarized.
Months 1, 3, 6, 12, 18, 24

その他の成果指標

結果測定
メジャーの説明
時間枠
Characterization of Procedure Details and Healthcare Utilization
時間枠:Months 1, 3, 6, 12, 18, 24.
Supportive data will be collected to characterize the index procedure and subsequent healthcare utilization. Procedure details include procedure time, anesthesia type, fluoroscopy time, and technical success. Healthcare utilization includes pain-related medication use, injections, additional interventions or reoperations, and pain-related healthcare visits from baseline through study completion. Data will be summarized descriptively.
Months 1, 3, 6, 12, 18, 24.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

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 (推定)

2026年7月1日

一次修了 (推定)

2027年12月1日

研究の完了 (推定)

2029年7月1日

試験登録日

最初に提出

2026年4月23日

QC基準を満たした最初の提出物

2026年4月23日

最初の投稿 (実際)

2026年4月30日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月23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21日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • PTQ-002

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Sponsored Study

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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