[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"femoral-acetabular-impingement\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:femoral-acetabular-impingement":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,72,96],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100638507","the-purpose-of-this-pilot-study-is-to-determine-feasibility-of-a-randomized-controlled-trial-comparing-labral-repair-versus-reconstruction-in-patients-over-40-years-of-age-undergoing-hip-arthroscopy-for-fais-100638507",false,"NCT07608237","The Purpose of This Pilot Study is to Determine Feasibility of a Randomized Controlled Trial Comparing Labral Repair Versus Reconstruction in Patients Over 40 Years of Age Undergoing Hip Arthroscopy for FAIS.","Labral Repair Versus Reconstruction in Symptomatic Femoroacetabular Impingement in Patients Over 40 Years of Age - A Randomized Controlled Trial","Inclusion:\n\n-Cam or pincer morphology who have failed a trial of conservative treatment\n\nExclusion:\n\n* Moderate concomitant OA (Tönnis 2+)\n* Have had previous hip surgery\n* Active joint or systemic infection\n* Significant muscle paralysis\n* Inflammatory arthropathies\n* Significant medical comorbidity that may alter effectiveness of surgical intervention\n* Active smoker\n* Major medical illness\n* Unable to speak and understand English\n* Psychiatric illness that precludes informed consent\n* Unwilling to be followed for 2 years","ALL","40 Years",{"count":19,"type":20},220,"ESTIMATED","INTERVENTIONAL",[23],"NA","The purpose of this pilot study is to determine feasibility of a randomized controlled trial comparing labral repair versus reconstruction in patients over 40 years of age undergoing hip arthroscopy for FAIS. Specifically, we aim to: (1) estimate the proportion of eligible patients providing consent, (2) estimate the magnitude of the between-groups difference in the primary outcome (International Hip Outcome Tool \\[iHOT\\] - 33) to aid in sample size calculation for the full study, (3) estimate the compliance in completing the proposed outcome measures to determine the burden of questionnaire completion.",[26],"Femoral Acetabular Impingement",[28,29],"labral repair","labral reconstruction","NOT_YET_RECRUITING","2026-05-19",{"date":33,"type":34},"2026-05-27","ACTUAL",{"date":36,"type":20},"2026-09-01",{"date":38,"type":20},"2028-12-31",{"name":40,"class":41},"Western University, Canada","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":42},"100628343","do-patient-characteristics-associate-with-poor-outcome-with-femoral-acetabular-impingement-syndrome-fais-following-physiotherapy-led-rehabilitation-100628343","NCT07460401","'Do Patient Characteristics Associate With Poor Outcome With Femoral Acetabular Impingement Syndrome (FAIS) Following Physiotherapy-led Rehabilitation'","Are Baseline Factors Associated With Persistent Pain in People With Femoral Acetabular Impingement Syndrome After a Physiotherapy-led Rehabilitation Programme?","FAIRO","Inclusion Criteria:\n\n* Participants aged between 18 and 55 years\n* Diagnosis of symptomatic FAIS following a formal clinical assessment - Appropriate imaging: MRI\u002FArthrogram, and \u002For Xray and\u002For CT (secondary care pathway for diagnosis but this is optional).\n* Awaiting PLR\n* No previous surgery to the index hip\n* Have capacity to give informed consent\n* English as a spoken language\n\nExclusion Criteria:\n\n* Presence of hip dysplasia, femoral stress fracture, synovitis or other inflammatory arthropathy (psoriatic arthropathy)\n* Kellgren-Lawrence grading of Osteoarthritis ≥2 (to exclude moderate OA which could be a confounding influence on pain)\n* Avascular necrosis of the femoral head\n* Previous surgery to index hip\n* Previous physiotherapy treatment to the index hip in the past 6 months\n* Current pregnancy\n* Perthes disease\n* Involved in a current research study involving the hip","18 Years","55 Years",{"count":54,"type":20},175,"OBSERVATIONAL","Background:\n\nThe hip joint is a ball and socket joint where the ball inserts into the socket. The ball shape is round but sometimes the ball has a bony bump on it. When the ball moves in the socket, the bump can hit the edge of the socket causing pain in movements like squatting or kicking a ball. Repeated hitting of the bump in the socket can cause hip pain, damage, and arthritis. This is called hip impingement and is found in 10-15% of young adults.\n\nDoes Physiotherapy treatment work? Exercises from a physiotherapist make the muscles stronger around the hip joint which alters the way the ball moves. This stops the bump hitting the socket and this can help reduce the pain. However, an experiment found only 32% of people doing exercises got better.\n\nSo, why after strengthening the muscles are some people still in pain? Is there another source of pain?\n\nOther causes of pain? The investigators know things like people's emotions such as 'feeling down' can affect pain. An experiment the investigators did, found neuropathic pain in people with hip impingement. This pain is caused by a disease of the nerves that provide information about your body. This can be a cause of pain even if your muscles are strong. In both situations, strengthening your muscles may not be the best choice. The investigators need to know more about types of pain in people with hip impingement to give better treatment.\n\nAim To look at causes of hip impingement in people before they have physiotherapy treatment, to see if the investigators can find a reason why some people don't get better after strengthening their muscles.\n\nProject design The investigators will review the research to see if people with hip impingement may feel for example, sad, anxious or scared of moving their hip, which could be a reason why some people don't get better after doing their strengthening exercises.\n\nThe investigators will invite 175 adults with hip impingement who have been referred for physiotherapy-led treatment to join this study. The participants will have 2 research appointments, 30-60 minutes each. The first one before the start of their physiotherapy treatment, the second one will be 4 months after starting their physiotherapy treatment. At both appointments the participants will complete special questionnaires designed to explore emotions and causes of pain. The investigators will compare the results of the questionnaires which will give more information about the causes of pain and how people view their pain. This will give the investigators a better understanding why strengthening exercises may not be the best treatment.\n\nPatient and public involvement (PPI) The investigators presented this project to 23 members of the public (who help researchers with their projects) at our monthly meeting. They thought this project was a good idea, especially talking about things like anxiety and depression. This will form part of the questionnaires.\n\nPatients told the investigators about their thoughts of having pain following treatment for hip pain. They felt further knowledge into why they had pain and help with mental and emotional support was important to them. They told the investigators about their concerns over the lack of information about what treatment can and cannot achieve. They were reluctant to suggest treatment.\n\nThree patients would like to help the investigators further design the study so that the information available to the public is clear and concise.",[26],[59,60,61,62],"Hip impingement","Patient characteristics","Outcomes","Physiotherapy-led rehabilitation","2026-03-27",{"date":65,"type":34},"2026-04-02",{"date":67,"type":20},"2026-04-06",{"date":69,"type":20},"2028-01-31",{"name":71,"class":41},"University of Oxford",{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":79,"sex":16,"minAge":51,"maxAge":17,"enrollmentInfo":80,"targetDuration":4,"studyType":21,"phases":82,"briefSummary":83,"conditions":84,"keywords":4,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":42},"100371237","blood-flow-restriction-following-hip-arthroscopy-100371237","NCT04113759","Blood Flow Restriction Following Hip Arthroscopy","Postoperative Blood Flow Restriction Training Following Hip Arthroscopy: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Adult patients 18-40\n* English-speaking\n* Clinical and radiographic examination (MRI) consistent FAIS and\u002For labral pathology, and are schedule for primary hip arthroscopy\n* Written and informed consent for study participation\n\nExclusion Criteria:\n\n* Patients younger than 18 or older than 40 years of age\n* Non-native English speaker\n* Revision surgery or prior history of ipsilateral hip or knee surgery\n* Inability to comply with the proposed follow-up clinic visits\n* Patients lacking decisional capacity\n* Patients with a history of deep vein thrombosis, pulmonary embolism, or known clotting disorder or hypercoagulable state\n* Pregnant or breast-feeding women. Pregnancy as determined by a positive pregnancy test prior to procedure. Females of childbearing potential must agree to use an acceptable birth control method during study participation.\n* Worker's compensation patients\n* Any clinically significant finding that would place the patient at health risk, impact the study, or affect the completion of the study\n* Any psychiatric illness that would prevent comprehension of the details and nature of the study and interfere with follow-up clinic visits",true,{"count":81,"type":20},56,[23],"This study will be a prospective randomized, double-blinded, placebo-controlled trial of patients undergoing primary hip arthroscopy for FAIS and\u002For labral pathology. All patients who sign the consent form will be enrolled in the study and randomized to one of the two treatment arms. Follow-up will take place at 1-month, 3-months, 6-months, and 1-year.",[85,26],"Labral Tear, Glenoid","RECRUITING","2025-12-04",{"date":89,"type":34},"2025-12-05",{"date":91,"type":34},"2023-08-01",{"date":93,"type":20},"2028-01",{"name":95,"class":41},"Rush University Medical Center",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":79,"sex":16,"minAge":51,"maxAge":103,"enrollmentInfo":104,"targetDuration":4,"studyType":21,"phases":106,"briefSummary":107,"conditions":108,"keywords":4,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":42},"100369773","hip-arthroscopy-postoperative-opioid-demands-100369773","NCT04094701","Hip Arthroscopy Postoperative Opioid Demands","Randomized Control Trial Evaluating Postoperative Opioid Demands Following Hip Arthroscopy","Inclusion Criteria:\n\n* Adult patients age 18-80 years\n* English speaking\n* Opioid naive patient (defined as not taking opioid pills within 6 weeks prior to surgery), confirmed by checking the Illinois Prescription monitoring program\n* Primary hip arthroscopy\n* Written and informed consent for study participation\n\nExclusion Criteria:\n\n* Minors (\\\u003C18 years of age)\n* Opioid tolerant patients\n* Revision surgery\n* Prior infections of the operative joint\n* History of active malignancy within the past 5 years\n* Chronic pain conditions including low back pain, chronic pain syndrome, fibromyalgia\n* History of alcohol or other substance use disorder\n* Other disease states including rheumatologic conditions, diabetes mellitus, hypo\u002Fhyperthyroidism, depression, anxiety\n* Grade IV chondral defects","80 Years",{"count":105,"type":20},170,[23],"This study will be a prospective, single-blinded, randomized controlled trial (RCT), investigating the influence of the number of opioid pills prescribed following primary hip arthroscopy. All patients who sign the consent form will be enrolled in the suited and randomized to one of the two treatment arms. The intervention group will receive 5 Norco pills, gabapentin (30 mg, once daily for 10 days following surgery), and Tylenol (1000 mg, three times daily for 10 days following surgery) while the control will receive the standard at our practice of 30 Norco pills.",[109,110,26,85],"Opioid Use","Pain","2025-08-05",{"date":113,"type":34},"2025-08-07",{"date":115,"type":34},"2020-10-21",{"date":117,"type":20},"2027-03",{"name":95,"class":41}]