[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sacroiliac-joint-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sacroiliac-joint-pain":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,67,96],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100635017","post-market-clinical-study-using-traq-for-minimally-invasive-posterior-sacroiliac-joint-fusion-100635017",false,"NCT07547215","Post-Market Clinical Study Using TRAQ™ for Minimally Invasive Posterior Sacroiliac Joint Fusion","An Open Label, Prospective, Multicenter, Single-Arm, Post-Market Clinical Study Using TRAQ™ for Minimally Invasive Posterior Sacroiliac Joint Fusion","TRAQTION","Inclusion Criteria:\n\nTo be eligible to participate in this study, a subject must meet all the following criteria, as determined by the Investigator:\n\n1. Age and Body Mass Index (BMI)\n\n   1. Adult patients aged ≥ 21 years at screening.\n   2. BMI ≤ 40.\n2. Chronic SIJ Related Pain\n\n   1. Has experienced low back and\u002For buttock pain for at least 6 months that has been inadequately responsive to non surgical management.\n   2. Has experienced nonradicular pain that is maximal below the L5 vertebrae, localized over the posterior SIJ, and consistent with SIJ pain.\n3. Diagnosis of SIJ Dysfunction\n\n   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 on 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.\n4. Baseline Disability and Pain Severity\n\n   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).\n5. Treatment Decision a. The treating physician has independently determined that the TRAQ 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.\n6. Informed Consent and Compliance\n\n   1. Is willing and capable of providing written informed consent; and\n   2. Is willing and able to comply with all study related requirements, procedures, and follow up visits.\n\nExclusion Criteria:\n\nSubjects must meet none of the following criteria to be eligible for participation in this study, as determined by the Investigator:\n\n1. Pain Source Uncertainty\n\n   a. Inability to confirm, in the Investigator's clinical judgment, that the subject's primary pain generator is the sacroiliac joint.\n2. Alternative Primary Spine Pathology\n\n   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.\n3. 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.\n4. Non SIJ Pain Syndromes\n\n   a. History of coccydynia or prior coccygectomy, endometriosis, cluneal neuralgia, or pudendal neuralgia.\n5. Recent Sacral Interventions\n\n   a. Prior sacral radiofrequency ablation performed within 6 months prior to enrollment.\n6. Recent Pelvic Trauma\n\n   a. History of major pelvic trauma within 12 months prior to enrollment.\n7. Severe Osteoporosis\n\n   a. Prior diagnosis or suspicion of severe osteoporosis, defined as a prior bone mineral density T score of \\\u003C -2.5 or a history of osteoporotic fracture.\n8. Medications Affecting Bone or Soft Tissue Healing\n\n   a. Current use of medications known to adversely affect bone quality or soft tissue healing, as determined by the Investigator.\n9. Anatomic Constraints\n\n   a. Anatomic anomalies or defects that, in the Investigator's opinion, would preclude safe or biomechanically appropriate device placement.\n10. Systemic Inflammatory or Rheumatologic Disease\n\n    a. Presence of a chronic inflammatory rheumatologic condition, such as rheumatoid arthritis.\n11. Centralized Pain Syndromes\n\n    a. Current diagnosis of fibromyalgia.\n12. Infection Risk\n\n    a. Evidence of current local or systemic infection that would increase surgical risk.\n13. High-Dose Opioid Therapy (≥90 MME\u002Fday)\n\n    a. Current use of systemic opioid analgesics at Screening\u002FBaseline with an average daily dose ≥90 morphine milligram equivalents (MME\u002Fday), based on medication reconciliation (prescription records and subject report) and standard MME conversion factors.\n14. Current Nicotine Use (Self-Reported)\n\n    a. Self-reported use of any nicotine-containing products (including smoking, vaping\u002Fe-cigarettes, cigars, pipes, smokeless tobacco, nicotine pouches, and nicotine replacement products) within 6 weeks prior to Screening\u002FBaseline.\n15. Secondary Gain or Litigation\n\n    a. Currently receiving or actively seeking workers' compensation or disability benefits or involved in injury related litigation.\n16. Pregnancy\n\n    a. Currently pregnant or planning to become pregnant within two (2) years following enrollment, as self reported.\n17. Vulnerable Populations\n\n    a. Individuals who are prisoners or wards of the state.\n18. Substance Abuse\n\n    a. Known or suspected active drug or alcohol abuse, including opioid misuse.\n19. Psychiatric Conditions\n\n    a. Diagnosed psychiatric disorder (e.g., schizophrenia, major depressive disorder, personality disorder) that, in the Investigator's judgment, could interfere with study participation.\n20. Concurrent Interventional Research\n\n    a. Current participation in another clinical trial.\n21. Neurologic Conditions Affecting Rehabilitation\n\n    a. Presence of a significant neurologic disorder that would interfere with participation in physical therapy or post procedural rehabilitation.\n22. 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.","ALL","21 Years",{"count":20,"type":21},100,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to evaluate the real-world performance, safety and efficacy of the TRAQ System.",[25,26],"Sacroiliac Joint Dysfunction","Sacroiliac Joint Pain","RECRUITING","2026-06-11",{"date":30,"type":31},"2026-06-15","ACTUAL",{"date":33,"type":31},"2026-05-27",{"date":35,"type":21},"2028-12",{"name":37,"class":38},"PainTEQ, LLC","INDUSTRY",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":55,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":4},"100635868","phase-4-linq-procedure-vs-conventional-medical-management-for-sacroiliac-dysfunction-100635868","NCT07558278","LINQ® Procedure vs. Conventional Medical Management for Sacroiliac Dysfunction","LINQT: An Open Label Randomized, Controlled, Multicenter, Prospective, Long Term Clinical Study on the Minimally Invasive Posterior Sacroiliac Fusion Device LINQ® System","LINQT","Inclusion Criteria:\n\n* To be eligible to participate in this study, a subject must meet ALL of the following criteria, as determined by the Investigator:\n\n  1. Age and Body Mass Index (BMI)\n\n     1. Adult subjects aged ≥ 21 years at screening.\n     2. BMI ≤ 40.\n  2. Chronic SIJ-Related Pain\n\n     1. Has experienced low back and\u002For buttock pain for at least 6 months that has been inadequately responsive to non-surgical management.\n     2. Has experienced nonradicular pain that is maximal below the L5 vertebrae, localized over the posterior SIJ, and consistent with SIJ pain.\n  3. Diagnosis of SIJ Dysfunction\n\n     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.\n  4. Baseline Disability and Pain Severity\n\n     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).\n  5. Nicotine Abstinence\n\n     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.\n  6. Treatment Decision\n\n     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.\n  7. Informed Consent and Compliance\n\n     1. Is willing and capable of providing written informed consent; and\n     2. Is willing and able to comply with all study-related requirements, procedures, and follow-up visits.\n\nExclusion Criteria:\n\n* Exclusion Criteria Subjects must meet none of the following criteria to be eligible for participation in this study, as determined by the Investigator:\n\n  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.\n  2. Alternative Primary Spine Pathology\n\n     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.\n  3. Other Sacroiliac Pathology\n\n     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.\n  4. Non-SIJ Pain Syndromes\n\n     a. History of coccydynia or prior coccygectomy, endometriosis, cluneal neuralgia, or pudendal neuralgia.\n  5. Recent Sacral Interventions\n\n     a. Prior sacral radiofrequency ablation performed within 6 months prior to enrollment.\n  6. Recent Pelvic Trauma\n\n     a. History of major pelvic trauma within 12 months prior to enrollment.\n  7. Severe Osteoporosis\n\n     a. Prior diagnosis or suspicion of severe osteoporosis, defined as a prior bone mineral density T-score of \\\u003C -2.5 or a history of osteoporotic fracture.\n  8. Medications Detrimental to Bone or Soft-Tissue Healing\n\n     a. Current use of medications known to adversely affect bone quality or soft-tissue healing, as determined by the Investigator.\n  9. Anatomic Constraints\n\n     a. Anatomic anomalies or defects that, in the Investigator's opinion, would preclude safe or biomechanically appropriate device placement.\n  10. Systemic Inflammatory or Rheumatologic Disease\n\n      a. Presence of a chronic inflammatory rheumatologic condition, such as rheumatoid arthritis.\n  11. Centralized Pain Syndromes\n\n      a. Current diagnosis of fibromyalgia.\n  12. Infection Risk\n\n      a. Evidence of current local or systemic infection that would increase surgical risk.\n  13. High-Dose Opioid Therapy (≥90 MME\u002Fday)\n\n      a. Current use of systemic opioid analgesics at Screening\u002FBaseline with an average daily dose ≥90 morphine milligram equivalents (MME\u002Fday), based on medication reconciliation (prescription records and subject report) and standard MME conversion factors.\n  14. Current Nicotine Use (Self-Reported)\n\n      a. Self-reported use of any nicotine-containing products (including smoking, vaping\u002Fe-cigarettes, cigars, pipes, smokeless tobacco, nicotine pouches, and nicotine replacement products) within 6 weeks prior to Screening\u002FBaseline.\n  15. Secondary Gain or Litigation\n\n      a. Currently receiving or actively seeking workers' compensation or disability benefits or involved in injury-related litigation.\n  16. Pregnancy\n\n      a. Currently pregnant or planning to become pregnant within two (2) years following enrollment, as self-reported.\n  17. Vulnerable Populations\n\n      a. Individuals who are prisoners or wards of the state.\n  18. Substance Abuse\n\n      a. Known or suspected active drug or alcohol abuse, including opioid misuse.\n  19. Psychiatric Conditions\n\n      a. Diagnosed psychiatric disorder (e.g., schizophrenia, major depressive disorder, personality disorder) that, in the Investigator's judgment, could interfere with study participation.\n  20. Concurrent Interventional Research\n\n      a. Current participation in another clinical trial.\n  21. Neurologic Conditions Affecting Rehabilitation\n\n      a. Presence of a significant neurologic disorder that would interfere with participation in physical therapy or post procedural rehabilitation.\n  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.",{"count":49,"type":21},200,"INTERVENTIONAL",[52],"PHASE4","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).",[26],[56,57],"sacroiliac joint dysfunction","LINQ","NOT_YET_RECRUITING","2026-05-13",{"date":61,"type":31},"2026-05-15",{"date":63,"type":21},"2026-07-01",{"date":65,"type":21},"2029-07-01",{"name":37,"class":38},{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":17,"minAge":74,"maxAge":75,"enrollmentInfo":76,"targetDuration":4,"studyType":50,"phases":78,"briefSummary":80,"conditions":81,"keywords":82,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":39},"100621411","cmct-versus-cse-in-treatment-of-sij-pain-100621411","NCT07370272","CMCT Versus CSE in Treatment of SIJ Pain","Lumbopelvic Cognitive Movement Control Training Versus Core Stability Exercises in Treatment of Sacroiliac Joint Pain","Inclusion Criteria:\n\n1. Age of the subjects will range between 18 - 45 years for young middle-aged adults.\n2. Unilateral SIJ pain lasting for at least 3 months, in lower back, buttock, groin, posterior superior iliac spine (PSIS) and with or without referral pain to the lower extremities.\n3. SIJ pain below L5 region.\n4. Non-centralized LBP i.e. has no directional preference.\n5. Score positive on 3 out of 5 SIJP provocation tests: compression, distraction, sacral thrust, thigh thrust, Gaenslen's.\n\nExclusion Criteria:\n\n1. Limb-length discrepancy,\n2. Clear signs of nerve root compression (radiating pain, motor and\u002For sensory deficits,\n3. Previous major back surgery or injury, fracture or arthritis of spine, pelvis, hip, knee or ankle joint,\n4. Seronegative spondyloarthropathies,\n5. Visual or vestibular deficit,\n6. Unable to follow command\u002F cognitive deficits,\n7. Postpartum women less than six months,","18 Years","45 Years",{"count":77,"type":21},36,[79],"NA","This study aims to investigate the difference between integrating lumbopelvic cognitive movement control training versus core stabilization exercises to the conventional physiotherapy program on pain, function, lumbopelvic stability, functional load transfer, and postural control in patients suffering from SIJ pain. The main question it aims to answer is:\n\nWhat are the effects of adding lumbopelvic movement control training versus core stabilization exercises to the conventional physiotherapy program in treating patients with SIJ pain?\n\nResearchers will compare adding lumbopelvic movement control training versus core stabilization exercises to the conventional physiotherapy program to investigate its effectiveness in treatment of SIJ pain\n\nParticipants will:\n\n1. receive the intervention as follows:\n\n   * Group (A) - Control Group: will receive conventional physiotherapy program (US and MET)\n   * Group (B) - Core Stability Exercises Group: will receive conventional US, MET, and core stability ex's\n   * Group (C) - Lumbopelvic cognitive movement control training Group: will receive conventional US, MET, and cognitive movement control training.\n2. receive the training protocol 3 times a week for 8 weeks according to the set schedules.\n3. perform a home exercise program in the same dose of repetitions and time as in the session.\n4. be assessed before and after the intervention and training period to address the outcome measures.",[26],[83,84,85],"cognitive movement control training","core stability exercises","sacroiliac joint pain","2026-01-19",{"date":88,"type":31},"2026-01-27",{"date":90,"type":21},"2026-02",{"date":92,"type":21},"2026-08",{"name":94,"class":95},"Cairo University","OTHER",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":11,"sex":17,"minAge":103,"maxAge":104,"enrollmentInfo":105,"targetDuration":4,"studyType":50,"phases":107,"briefSummary":108,"conditions":109,"keywords":110,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":4},"100574629","combined-corticosteroid-injections-and-shockwave-therapy-for-sacroiliac-joint-pain-100574629","NCT06761768","Combined Corticosteroid Injections and Shockwave Therapy for Sacroiliac Joint Pain","Efficacy of Combining Corticosteroid Injections and Extracorporeal Shockwave Therapy in Patients With Sacroiliac Joint Pain","Inclusion Criteria:\n\n* Low back pain lasting for 3 months or more\n* Pain VAS score of 4 or higher\n* Three or more positive results in sacroiliac joint provocation tests\n* At least 50% pain relief following ultrasound-guided sacroiliac joint injection with local anesthetic\n\nExclusion Criteria:\n\n* Currently undergoing extracorporeal shockwave therapy in other areas\n* Suspected pain caused by other lumbar spine or hip joint conditions (e.g., lumbar spine or disc disorders, radicular pain, spondylolisthesis\u002Fdisc degeneration, hip arthritis)\n* Presence of complex comorbidities, including trauma, systemic infections (e.g., fever, chills, night sweats), local sacroiliac joint infections, autoimmune diseases, or immunosuppression\n* Sacroiliac joint injection therapy received within the past 6 months\n* Contraindications for extracorporeal shockwave therapy (e.g., cancer or current\u002Fprior infections at the treatment site, pacemakers, pregnancy, epilepsy, or coagulation disorders caused by disease or medication)\n* Impaired renal function preventing the administration of contrast agents for sacroiliac joint bone scanning","20 Years","75 Years",{"count":106,"type":21},44,[79],"This study aims to investigate the combined use of corticosteroid injections and ESWT for SIJ pain.",[25,26],[25,111,112,113],"Sacroiliac joint pain","Steroid Injection","Extracorporeal shock wave therapy","2025-01-07",{"date":116,"type":31},"2025-01-09",{"date":118,"type":21},"2025-08-01",{"date":120,"type":21},"2026-07-31",{"name":122,"class":95},"Tri-Service General Hospital"]