[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hip-arthroscopy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hip-arthroscopy":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,48,84,107,133,156],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100595856","phase-4-efficacy-of-ketorolac-for-postoperative-pain-management-in-hip-arthroscopy-100595856",false,"NCT07037888","Efficacy of Ketorolac for Postoperative Pain Management in Hip Arthroscopy","Efficacy of Ketorolac for Postoperative Pain Management in Hip Arthroscopy: A Prospective, Randomized, Clinical Trial","Inclusion Criteria:\n\n* Patients undergoing hip arthroscopy over the age of 18 with Dr. T. Sean Lynch\n* Diagnosis of femoroacetabular impingement (FAI)\n\nExclusion Criteria:\n\n* Patients with inability to consent and\u002For do not speak English\n* Patients with conditions contraindicated with NSAIDs (medication allergy, peptic ulcer disease, bleeding diathesis, and renal disease)\n* Patients with history of drug and alcohol use disorder\n* Patients with chronic analgesia (filled two opioid prescriptions within 6 months of the surgery)\n* Patients with psychotropic medication usage\n* Patients who take pentoxifylline, probonecid, aspirin, and\u002For NSAIDs who cannot stop taking it for the study\n* Patients who are not discharged same day after surgery","ALL","18 Years","89 Years",{"count":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"PHASE4","The goal of this clinical trial is to learn whether the medication ketorolac can help manage pain after hip arthroscopy as well or better than the standard opioid-based pain medications. This study focuses on adult patients (over 18 years old) undergoing hip arthroscopy at Henry Ford Health System in Detroit, Michigan. Both men and women are included, and all participants must be able to consent and communicate in English.\n\nThe main questions it aims to answer are:\n\nCan ketorolac help control pain as effectively or better than opioids after hip arthroscopy?\n\nWill ketorolac use reduce the amount of opioid medication needed after surgery?\n\nResearchers will compare the group receiving ketorolac to the group receiving standard opioid pain medications to see if ketorolac reduces pain and opioid use after surgery.\n\nParticipants will:\n\nBe randomly assigned to one of two groups:\n\nThe control group, which receives the current standard pain management protocol (hydrocodone-acetaminophen and diazepam)\n\nThe experimental group, which receives the same protocol plus ketorolac and a stomach-protecting medication (omeprazole)\n\nReceive their assigned pain medications after hip arthroscopy\n\nBe asked to:\n\nTake the prescribed medications after discharge\n\nComplete a pain journal for 5 days following surgery, documenting pain levels and any side effects\n\nComplete follow-up surveys and assessments at 2 weeks, 6 weeks, and 3 months after surgery\n\nThe main measurement researchers will use is the Visual Analog Scale (VAS) for pain on post-operative day 4. Additional measures include how many narcotic pills are used and results from PROMIS physical function and pain interference scores.\n\nThe hope is that ketorolac will provide equal or better pain control without the risks of addiction and side effects associated with opioid medications. If successful, this approach could offer a safer alternative for managing pain after hip arthroscopy. Participants may personally benefit by having effective pain relief with fewer risks, and future patients could benefit from improved pain management options.",[27,28],"Femoracetabular Impingement","Hip Arthroscopy",[30,28,31,32,33,34],"Sports Medicine","FAI","Opioids","Ketorolac","Multi-modal pain","RECRUITING","2026-06-26",{"date":38,"type":39},"2026-06-30","ACTUAL",{"date":41,"type":39},"2023-12-13",{"date":43,"type":21},"2026-12",{"name":45,"class":46},"Henry Ford Health System","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":47},"100594505","phase-2-brain-computer-interface-visualization-training-to-optimize-muscle-activation-following-orthopaedic-surgery-100594505","NCT07020312","Brain-Computer Interface Visualization Training to Optimize Muscle Activation Following Orthopaedic Surgery","Brain-Computer Interface Visualization Training to Optimize Muscle Activation Following Orthopaedic Surgery: A Blinded Randomized Controlled Trial","iBrainTechRCT","Participants\n\n* Inclusion Criteria:\n\n  * Patient age \\>18 years\n  * Ability to complete neurofeedback training and follow study follow-ups\n  * Indicated for one of the four investigated orthopedic procedures\n* Exclusion Criteria:\n\n  * Inability to participate in neurofeedback training\n  * Lack of decisional capability\n  * History of stroke, movement disorder (e.g. Parkinson's), peripheral neuropathy\n  * Cardiac pacemaker or other internal electronic device\n  * BMI \\>35\n  * Previous surgery or specific pathology on the affected joint (refer to procedure specific indications below)\n\nProcedure Specifics:\n\nAnterior cruciate ligament reconstruction (ACLR) Procedure-specific Inclusion Criteria\n\n* Patients undergoing primary ACLR with autograft or allograft tissue\n* Adjunct lateral Extra-articular tenodesis will be included\n* Additional meniscus debridement and repair will be included Procedure-specific exclusion criteria\n* Revision ACL surgery\n* Moderate to Severe arthritis - Kellgren-Lawerence (KL) Grade \\> 3\n* Patients with meniscus root repair\n* Non-weight-bearing status exceeding 1 week postoperatively\n\nTotal knee arthroplasty (TKA) Procedure specific inclusion criteria\n\n* Patients undergoing primary TKA\n* Preoperative total knee range of motion of at least 100 degrees (combined flexion and extension)\n* Prior extensor mechanism tendon repair, quadriceps or patella tendon. Procedure specific exclusion criteria\n* Revision surgery\n* Hinged implant\n* Any open procedure involving the knee joint\n* Symptomatic arthritis in the contralateral knee with planned or expected total knee arthroplasty within 6 months\n* Inflammatory Arthritis\n\nTotal hip arthroplasty (THA) Procedure Specific Inclusion Criteria\n\n* Patients undergoing primary THA Procedure Specific Exclusion Criteria\n* Revision Surgery\n* Any open procedure involving the hip joint\n* Bilateral THA procedures\n* Inflammatory Arthritis\n\nHip arthroscopy (HA) for femoroacetabular impingement syndrome (FAIS) Procedure Specific Inclusion Criteria\n\n· Patients undergoing HA for FAIS Procedure Specific Exclusion Criteria\n\n* Revision Surgery\n* Diagnosis of hip dysplasia",{"count":57,"type":21},240,[59],"PHASE2","After orthopedic surgeries like knee or hip replacement, some patients struggle to fully activate their muscles due to a condition called Arthrogenic Muscle Inhibition (AMI). AMI can slow recovery and make physical therapy less effective. This clinical trial is testing whether a special type of brain training-called neurofeedback visualization training-can help improve muscle activation and speed up recovery.\n\nIn this study, patients will receive standard physical therapy after surgery. Half of them will also use a device that helps them \"visualize\" exercises while wearing a cap that reads brain signals (EEG). The cap tracks brain activity when patients imagine doing specific movements. A computer then shows a virtual avatar performing the movements, giving feedback in real time-like a video game controlled by the brain.\n\nThe study includes patients recovering from one of four surgeries:\n\n1. Anterior cruciate ligament reconstruction (ACLR)\n2. Total knee arthroplasty (TKA)\n3. Total hip arthroplasty (THA)\n4. Hip arthroscopy (HA) for femoroacetabular impingement (FAI)\n\nThe goal is to see if this training improves muscle strength, movement, and daily function more than standard therapy alone. The study will take place at Rush University Medical Center in Chicago and enroll 240 adults, with 60 patients per type of surgery. Each participant will be followed for up to 6 months after surgery and complete strength tests, movement assessments, and questionnaires about their recovery.\n\nThe hope is that combining brain training with physical therapy will lead to faster, more complete recoveries and improve how patients move after surgery.",[62,63,64,28],"Anterior Cruciate Ligament Reconstruction","Total Hip Arthroplasty (THA)","Total Knee Arthroplasty",[66,67,68,28,69,70,71,72,73,74],"ACLR","THA","TKA","Arthrogenic muscle inhibition","Electroencephalography","Gait","Motion Analysis","Biomechanics","Strength","2026-06-17",{"date":77,"type":39},"2026-06-18",{"date":79,"type":39},"2025-08-14",{"date":81,"type":21},"2028-08-01",{"name":83,"class":46},"Rush University Medical Center",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":16,"minAge":91,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":94,"phases":4,"briefSummary":95,"conditions":96,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":47},"100496615","an-evaluation-of-hip-preservation-outcomes-100496615","NCT05746533","An Evaluation of Hip Preservation Outcomes","A Comparison of Total Hip Arthroplasty and Hip Preservation Outcomes","Inclusion Criteria:\n\n* Candidates for surgical intervention of the hip\n* Participant and\u002For guardian has given informed consent and assent as applicable.\n\nExclusion Criteria:\n\n* Documented history of pre-existing hip conditions (SCFE, LCPD, acetabular fractures)\n* Has language or cognitive barriers preventing understanding of study and consent and assent documents\n* Prior revision surgeries\n* Patients from the trauma\u002Femergency department\n* Individuals with Unusable x-rays","12 Years",{"count":93,"type":21},10000,"OBSERVATIONAL","The purpose of this study is to assess outcomes of hip preservation surgeries including open and arthroscopic treatment of femoroacetabular impingement (FAI).",[28,97],"Femoroacetabular Impingement","2026-05-15",{"date":100,"type":39},"2026-05-19",{"date":102,"type":39},"2023-06-02",{"date":104,"type":21},"2053-06",{"name":106,"class":46},"Yale University",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":22,"phases":118,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":47},"100470148","phase-1-amic-compared-with-microfracture-for-focal-articular-cartilage-damage-of-the-hip-100470148","NCT05402072","AMIC Compared With Microfracture for Focal Articular Cartilage Damage of the Hip","Autologous MatRix-Induced ChondrogenEsis ComPared With Microfracture for Focal ArtIcular CaRtilage Damage of the Hip (REPAIR): A Pilot Randomized Controlled Trial","REPAIR","Inclusion Criteria:\n\n1. All patients aged 18-55 years\n2. Hip pain lasting 6 months or more with no relief from documented non-operative modalities\n3. Focal articular cartilage defects of the acetabulum on MRI, confirmed to be full thickness (International Cartilage Regeneration and Joint Preservation Society (ICRS) grade 3 or 4) during arthroscopic examination\n4. Focal acetabular articular cartilage lesions measuring between 3 cm2 and 25 cm2 on MRI and confirmed on arthroscopic examination\n5. Patient agrees to participate in the study-specific postoperative rehabilitation protocol\n6. Patient can speak, read, and understand the language of the site\n7. Patient has provided informed consent\n\nExclusion Criteria:\n\n1. Cartilage defects of the femoral head\n2. Previous surgery on the study hip\n3. Traumatic chondral injury of the hip from a single event\n4. Presence of advanced osteoarthritis (Tonnis grade 3) or any other acute or chronic inflammatory joint disease\n5. Known hypersensitivity or allergy to porcine collagen\n6. Acute or chronic infection at the surgical site\n7. Evidence of hip dysplasia (i.e., lateral centre edge angle \\\u003C 20˚)\n8. Evidence of acetabular over coverage such as coxa profunda or coxa protrusion\n9. Immunosuppressive or anti-proliferative medication use\n10. Chronic pain syndromes\n11. Significant medical co-morbidities (requiring assistance for activities of daily living (ADLs))\n12. History of paediatric hip disease\n13. Uncontrolled diabetes\n14. Contraindications to MRI imaging (e.g. claustrophobia)\n15. Patient is involved in ongoing legal or workplace claims\n16. Patient is incarcerated\n17. Patient is pregnant or breastfeeding\n18. Patient who will likely have problems, in the judgement of the investigator, with maintaining follow-up\n19. Any other reason(s) the investigator feels is relevant for excluding the patient","55 Years",{"count":117,"type":21},40,[119],"PHASE1","This is a pilot multi-centre RCT of 40 patients (ages 18-55 years, inclusive) undergoing primary hip arthroscopy with a focal articular cartilage defect of the acetabulum to compare the effect of using autologous matrix-induced chondrogenesis (AMIC) in comparison to microfracture on hip function, health-related quality of life, hip pain, cartilage regeneration, health utility, and any adverse events at 2 years. Follow-up will occur at 6 weeks, 6 months, 12 months, 18 months, and 24 months post-surgery.",[28,122,123],"Articular Cartilage Defect","Microfractures","2025-09-22",{"date":126,"type":39},"2025-09-24",{"date":128,"type":39},"2023-03-13",{"date":130,"type":21},"2027-01-01",{"name":132,"class":46},"McMaster University",{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":137,"acronym":138,"eligibilityCriteria":139,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":140,"enrollmentInfo":141,"targetDuration":4,"studyType":22,"phases":143,"briefSummary":145,"conditions":146,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":47},"100588155","analysis-of-biomechanical-parameters-and-return-to-sport-after-hip-arthroscopy-100588155","NCT06937710","Analysis of Biomechanical Parameters and Return to Sport After Hip Arthroscopy","ATH","Inclusion Criteria:\n\n* Hip arthroscopy for labrum lesion\n* athlete prior to arthroscopy with desire to return to sport\n\nExclusion Criteria:\n\n* Previous surgery or pathology of the operated lower limb\n* Contralateral hip operated\n* Neurological pathology affecting movement\n* Medical condition contraindicating participation in sports\n* Dementia or inability to complete questionnaires and assessments\n* Pregnant or breast-feeding patient\n* Patient under protective supervision\n* Patient not covered by a social security scheme","50 Years",{"count":142,"type":21},50,[144],"NA","The aim of this prospective study is to describe dynamic movement parameters in active patients who underwent surgery between 3 and 6 months after hip arthroscopy, focusing on movements such as jumping, squatting and acceleration. By examining the relationships between these different parameters and the return to sporting activities, and by integrating different angle and alignment measurements per- and post-operatively, we hope to find predictive factors for successive rehabilitation in athletes, which could lead to more personalized rehabilitation protocols.",[28],"2025-06-10",{"date":149,"type":39},"2025-06-11",{"date":151,"type":39},"2025-04-17",{"date":153,"type":21},"2026-07-31",{"name":155,"class":46},"Clinique du Sport, Bordeaux Mérignac",{"id":157,"slug":158,"hasResults":11,"nctId":159,"briefTitle":160,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":163,"targetDuration":4,"studyType":22,"phases":164,"briefSummary":165,"conditions":166,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":172,"completionDateStruct":174,"leadSponsor":176,"locationsCount":47},"100581086","absorbable-vs-non-absorbable-sutures-for-hip-capsular-closure-100581086","NCT06845735","Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure","Prospective Randomized Control Trial Comparing Absorbable Sutures to Non-Absorbable Sutures for Capsular Closures in Hip Arthroscopies","Inclusion Criteria:\n\n* Subjects 18 years of age and older.\n* Subject requiring surgical hip arthroscopic intervention for their hip pathology\n\nExclusion Criteria:\n\n* Subjects less than 18 years of age.\n* Subjects with any other medical problem precluding anesthesia or surgery.\n* Unable to provide informed consent.",{"count":20,"type":21},[144],"The study is to prospectively compare absorbable sutures with non-absorbable sutures used for capsular repair during hip arthroscopic procedures. Major outcomes will be measured using three questionnaires ((1) International Hip Outcome Tool-12 (iHOT-12), (2) modified Harris hip score, (3) hip outcome score) in addition to the standard of care set of 9 questionnaires. The other major outcome will be any radiographic heterotrophic ossification at the 6-month follow-up time point.",[167,28,168],"Labrum Injury of the Hip Joint","Femoroacetabular Impingement Syndrome","2025-05-01",{"date":171,"type":39},"2025-05-04",{"date":173,"type":39},"2024-03-22",{"date":175,"type":21},"2028-01-01",{"name":177,"class":46},"University of Missouri-Columbia"]