[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hip-injuries\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hip-injuries":251},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,59,93,116,136,159,183,205,225],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":13,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":16,"targetDuration":4,"studyType":19,"phases":4,"briefSummary":20,"conditions":21,"keywords":36,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":47,"lastUpdatePostDateStruct":48,"startDateStruct":51,"completionDateStruct":53,"leadSponsor":55,"locationsCount":58},"100434493",false,"NCT04937868","Developing a Decision Instrument to Guide Abdominal-pelvic CT Imaging of Blunt Trauma Patients","NEXUS AP CT","Inclusion Criteria:\n\nBlunt trauma patients who undergo abdominal-pelvic CT imaging during their initial trauma evaluation in the emergency department.\n\nExclusion Criteria:\n\nNone","ALL",{"count":17,"type":18},12000,"ESTIMATED","OBSERVATIONAL","Unrecognized abdominal and pelvic injuries can result in catastrophic disability and death. Sporadic reports of \"occult\" injuries have generated concern, and physicians, fearing that they may miss such an injury, have adopted the practice of obtaining computed tomography on virtually all patients with significant blunt trauma. This practice exposes large numbers patients to dangerous radiation at considerable expense, while detecting injuries in a small minority of cases.\n\nExisting data suggest that a limited number of criteria can reliably identify blunt injury victims who have \"no risk\" of abdominal or pelvic injuries, and hence no need for computed tomography (CT), without misidentifying any injured patient. It is estimated that nationwide implementation of such criteria could result in an annual reduction in radiographic charges of $75 million, and a significant decrease in radiation exposure and radiation induced malignancies.\n\nThis study seeks to determine whether \"low risk\" criteria can reliably identify patients who have sustained significant abdominal or pelvic injuries and safely decrease CT imaging of blunt trauma patients. This goal will be accomplished in the following manner:\n\nAll blunt trauma victims undergoing computed tomography of the abdomen\u002Fpelvis in the emergency department will undergo routine clinical evaluations prior to radiographic imaging. Based on these examinations, the presence or absence of specific clinical findings (i.e. abdominal\u002Fpelvic\u002Fflank pain, abdominal\u002Fpelvic\u002Fflank tenderness, bruising abrasions, distention, hip pain, hematuria, hypotension, tachycardia, low or falling hematocrit, intoxication, altered sensorium, distracting injury, positive FAST imaging, dangerous mechanism, abnormal x-ray imaging) will be recorded for each patient, as will the presence or absence of abdominal or pelvic injuries. The clinical findings will serve as potential imaging criteria. At the completion of the derivation portion of the study the criteria will be examined to find a subset that predicts injury with high sensitivity, while simultaneously excluding injury, and hence the need for imaging, in the remaining patients. These criteria will then be confirmed in a separate validation phase of the study.\n\nThe criteria will be considered to be reliable if the lower statistical confidence limit for the measured sensitivity exceeds 98.0%. Potential reductions in CT imaging will be estimated by determining the proportion of \"low-risk\" patients that do not have significant abdominal or pelvic injuries.",[22,23,24,25,26,27,28,29,30,31,32,33,34,35],"Abdominal Injury","Pelvic Fracture","Genital Hemorrhage","Lumbar Spine Injury","Hip Injuries","Liver Injury","Spleen Injury","Renal Injury","Diaphragm Injury","Aortic Rupture","Aortic Dissection","Bowel Disease","Vascular System Injuries","Sacral Fracture",[37,38,39,40,41,42,43,44,45],"Blunt trauma","Abdominal injury","Pelvic injury","Spine injury","Genital injury","Vascular injury","Hip injury","Computed tomography","Decision instrument","RECRUITING","2026-01-09",{"date":49,"type":50},"2026-01-13","ACTUAL",{"date":52,"type":50},"2018-01-15",{"date":54,"type":18},"2027-06-15",{"name":56,"class":57},"University of California, Los Angeles","OTHER",1,{"id":60,"slug":4,"hasResults":10,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":4,"eligibilityCriteria":64,"healthyVolunteers":65,"sex":15,"minAge":66,"maxAge":67,"enrollmentInfo":68,"targetDuration":4,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":77,"overallStatus":83,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":58},"100615817","NCT07297537","Adductor Endurance Test: Validity and Reliability","Validity and Reliability of the Adductor Endurance Test Developed for the Hip Adductor Muscles","Inclusion Criteria:\n\n* Being between 18 and 30 years of age\n* Being a professional soccer player for at least four years\n* Actively participating in training sessions\n* Scoring \\>87.5 points on the hip and groin injury questionnaire (HAGOS) sports subscale\n\nExclusion Criteria:\n\n* Having any orthopedic injury involving the lower extremities that would prevent participation in training sessions\n* Experiencing pain rated four or higher on the numerical pain rating scale during the hip adductor squeeze test and palpation of the adductor muscle tendons.",true,"18 Years","30 Years",{"count":69,"type":18},18,"INTERVENTIONAL",[72],"NA","Groin and hip injuries are common in team sports-especially soccer, rugby, and ice hockey-and frequently affect male and young athletes. About 14% of all sports injuries involve the groin and hip region, with most related to the adductor muscles. These injuries often increase during congested match periods and may result in athletes missing 1 to 6.9 weeks of training or competition, extending up to 14 weeks when surgery is required. Weakness in the adductor muscles is a key risk factor for groin injuries, and current assessments primarily measure maximal strength using tools such as squeeze tests, sphygmomanometers, or dynamometers. However, muscle endurance-critical because many injuries occur under fatigue-has not been adequately studied, and no validated endurance tests for the hip adductors exist. This study aims to evaluate the validity and reliability of a newly developed hip adductor endurance test for monitoring endurance strength in professional soccer players.",[75,26,76],"Groin Injury","Athletic Injuries",[78,79,80,81,82],"Hip adductor muscles","Adductor endurance","Sports injuries","Validity","Reliability","NOT_YET_RECRUITING","2025-12-23",{"date":86,"type":50},"2025-12-30",{"date":88,"type":18},"2026-04-15",{"date":90,"type":18},"2026-10-15",{"name":92,"class":57},"Izmir Democracy University",{"id":94,"slug":4,"hasResults":10,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":4,"eligibilityCriteria":98,"healthyVolunteers":65,"sex":15,"minAge":99,"maxAge":67,"enrollmentInfo":100,"targetDuration":4,"studyType":70,"phases":102,"briefSummary":103,"conditions":104,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":115},"100476754","NCT05488054","Muscle O2 Saturation and Hemoglobin Levels During Rehabilitation From Arthroscopic Surgery","Use of a Wearable Muscle Oxygen Saturation Sensor in the Rehabilitation of High-School and Collegiate Athletes Recovering From Arthroscopic Hip and Knee Surgery","Inclusion Criteria:\n\n* Age range: Patients age 14 to 30 years\n* Patients with ACL injury requiring surgical correction\n* Patients undergoing arthroscopic hip surgery\n* Healthy individuals with no history of ACL, arthroscopic knee or arthroscopic hip surgery\n\nExclusion Criteria:\n\n* Patients below 14 years or above 30 years\n* Non-English-speaking subjects\n* Pregnant individuals","14 Years",{"count":101,"type":18},226,[72],"This study will utilize the Moxy wearable sensor to measure muscle oxygen saturation levels in athletes following lower extremity surgery (ACL or Hip arthroscopy) to evaluate their Return-to-Play. The acquired data will complement current protocols utilized by Dr. Voos and Dr. Salata in this regard and will add quantifiable evidence to enable a robust measurement of the surgical limb versus non-surgical limb.",[105,26],"ACL Injury","2025-12-22",{"date":108,"type":50},"2025-12-24",{"date":110,"type":50},"2022-08-08",{"date":112,"type":18},"2026-12",{"name":114,"class":57},"University Hospitals Cleveland Medical Center",2,{"id":117,"slug":4,"hasResults":10,"nctId":118,"briefTitle":119,"officialTitle":119,"acronym":120,"eligibilityCriteria":121,"healthyVolunteers":10,"sex":15,"minAge":66,"maxAge":4,"enrollmentInfo":122,"targetDuration":4,"studyType":70,"phases":124,"briefSummary":125,"conditions":126,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":58},"100521020","NCT06064136","Psoas Tenotomy Under Ultrasound","TEPSe","Inclusion criteria:\n\n* Patients 18 years of age or older\n* Indication of psoas tenotomy for ilio-psoas conflict after total hip replacement\n* Signature of the written informed consent form by the patient\n* Affiliation to a French health insurance scheme or equivalent\n\nNon Inclusion criteria:\n\n* Vulnerable people: pregnant or breast-feeding women (patients will undergo a pregnancy test: urinary test), adult under guardianship or deprived of freedom.\n* Allergies to local anesthetics\n* Patient on anticoagulant or antiplatelet agents\n* Contraindication to surgery\n* Refusal of patient involvement",{"count":123,"type":18},15,[72],"The ilio-psoas conflict is a commonly accepted complication after total hip replacement, often linked to a mispositioning of the acetabular prosthetic component that conflicts with the ilio-psoas tendon. To correct these pains, a psoas tenotomy can be proposed. The results proven by the literature are very satisfactory. Psoas tenotomy is performed endoscopically, arthroscopically, or more rarely open.\n\nThe contribution of echo surgery allows to limit the scar ransom but also to free itself from a complex infrastructure to the operating room including an arthroscopy column and an intraoperative fluoroscopy for a conventional tenotomy, This also saves procedural and installation time.\n\nNo studies to date have described ultrasound-assisted psoas tenotomy Yhe investigators conducted a cadaveric study of the feasibility of psoas tenotomy under ultrasound that confirms the feasibility of this technique and the safety of the gesture for the surrounding anatomical structures.\n\nThe objectives of this study are to assess the feasibility, pain and functional outcomes of ultrasound-assisted psoas tenotomy in patients with ilio-psoas conflict after total hip replacement.",[26],"2025-11-27",{"date":129,"type":50},"2025-12-04",{"date":131,"type":18},"2025-12",{"date":133,"type":18},"2026-09",{"name":135,"class":57},"Centre Hospitalier Universitaire de Nice",{"id":137,"slug":4,"hasResults":10,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":10,"sex":15,"minAge":66,"maxAge":4,"enrollmentInfo":142,"targetDuration":4,"studyType":19,"phases":4,"briefSummary":144,"conditions":145,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":158},"100540752","NCT06320925","SportsPro: Post-Market Clinical Follow Up Study","A Retrospective, Multi-Center, Post-Market Clinical Follow-Up Study of Stryker Class IIb Implants","Inclusion Criteria:\n\n1. Subject was ≥ 18 years of age at the time of the surgery\n2. Subject has undergone joint space repair using one of the study devices\n\nExclusion Criteria:\n\n1. Subjects who are less than 6 months post-intervention\n2. Concurrent participation in an investigational clinical study during the study period",{"count":143,"type":18},1500,"Retrospective, multi-center, chart review (only to include data that is part of the surgeons' standard practice)",[146,147,26],"Shoulder Injuries","Knee Injuries","2025-05-22",{"date":150,"type":50},"2025-05-29",{"date":152,"type":50},"2023-12-05",{"date":154,"type":18},"2026-12-01",{"name":156,"class":157},"Stryker Endoscopy","INDUSTRY",3,{"id":160,"slug":4,"hasResults":10,"nctId":161,"briefTitle":162,"officialTitle":163,"acronym":4,"eligibilityCriteria":164,"healthyVolunteers":10,"sex":15,"minAge":66,"maxAge":4,"enrollmentInfo":165,"targetDuration":4,"studyType":70,"phases":167,"briefSummary":168,"conditions":169,"keywords":171,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":158},"100434233","NCT04934462","Evaluation of Non-Surgical and Arthroscopic Treatment for Hip Microinstability","Prospective Evaluation of Non-Surgical and Arthroscopic Treatment for Hip Microinstability","Inclusion Criteria:\n\n* Hip microinstability\n* Minimum 18 years old\n\nExclusion Criteria:\n\n* Hip osteoarthritis\n* Severe hip dysplasia\n* Perthes disease or avascular necrosis of the femoral head\n* Previous surgery to the hip joint",{"count":166,"type":18},26,[72],"Microinstability of the hip joint is an important cause of hip pain and reduced hip function in young and active individuals. Hip microinstability is due to extraphysiologic hip motion and could be secondary to acetabular dysplasia, connective tissue disorder, macrotrauma, microtrauma, iatrogenic- and idiopathic causes. Treatment for hip microinstability is initiated with non-surgical treatment consisting of physiotherapy aimed mainly at stability. If non-surgical treatment fails, surgery with arthroscopic plication of the hip joint capsule is the preferred method. This study evaluates non-surgical and arthroscopic treatment for hip microinstability regarding hip function and adverse events.",[170,26],"Musculoskeletal Abnormalities",[172,173],"arthroscopy","physiotherapy","2025-03-11",{"date":176,"type":50},"2025-03-12",{"date":178,"type":50},"2021-11-26",{"date":180,"type":18},"2026-01",{"name":182,"class":57},"Göteborg University",{"id":184,"slug":4,"hasResults":10,"nctId":185,"briefTitle":186,"officialTitle":187,"acronym":4,"eligibilityCriteria":188,"healthyVolunteers":10,"sex":15,"minAge":66,"maxAge":4,"enrollmentInfo":189,"targetDuration":4,"studyType":19,"phases":4,"briefSummary":191,"conditions":192,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":197,"lastUpdatePostDateStruct":198,"startDateStruct":199,"completionDateStruct":201,"leadSponsor":203,"locationsCount":158},"100364703","NCT04028687","MDR - PMCF Study for Taperloc Complete Stems","Post Market Clinical Follow up Study to Provide Safety, Performance and Clinical Benefits Data of the Taperloc Complete Stems","Inclusion Criteria:\n\n* Patient must be 18 years of age or older and skeletally mature\n* Patient must be willing and able to sign IRB approved informed consent\n* Patient must have undergone primary or revision hip arthroplasty with the -Taperloc Complete stem according to a cleared indication, which includes the following:\n* Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis\n* Rheumatoid arthritis\n* Correction of functional deformity\n* Treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable by other techniques\n\nExclusion Criteria:\n\n* Off-label use\n* Infection\n* Sepsis\n* Osteomyelitis\n* Uncooperative patient or patient with neurologic disorders who are incapable of following directions\n* Osteoporosis\n* Metabolic disorders which may impair bone formation\n* Osteomalacia\n* Distant foci of infections which may spread to the implant site\n* Rapid joint destruction, marked bone loss or bone resorption apparent on roentgenogram\n* Vascular insufficiency, muscular atrophy, or neuromuscular disease\n* Patient is known to be pregnant or nursing\n* Patient is a prisoner\n* Patient is a known alcohol or drug abuser\n* Patient has a psychiatric illness or cognitive deficit that will not allow for proper informed consent",{"count":190,"type":18},820,"The objective of this consecutive series PMCF study is to collect data confirming safety, performance, and clinical benefits of the Taperloc Complete stems when used for primary or revision total hip arthroplasty (implants) at 1,3,5,7 and 10-year follow-up\\*. Since Taperloc Complete was introduced to the EU in 2010, all available retrospective data will be collected from each patient and a prospective aspect to the study will be necessary to reach the 10-year time point.",[193,194,195,26,196],"Hip Arthritis","Hip Disease","Hip Fractures","Hip Pain Chronic","2025-03-10",{"date":174,"type":50},{"date":200,"type":50},"2020-02-13",{"date":202,"type":18},"2032-02-12",{"name":204,"class":157},"Zimmer Biomet",{"id":206,"slug":4,"hasResults":10,"nctId":207,"briefTitle":208,"officialTitle":208,"acronym":4,"eligibilityCriteria":209,"healthyVolunteers":10,"sex":15,"minAge":66,"maxAge":210,"enrollmentInfo":211,"targetDuration":4,"studyType":70,"phases":213,"briefSummary":214,"conditions":215,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":58},"100452009","NCT05165927","Comparison of Methods in Post Operative Hip Arthroscopy Rehabilitation","Inclusion Criteria:\n\n* patients with labral tears, femoroacetabular impingement syndrome, loose bodies, ligamentum teres tears, and related intra-articular pathology to be treated with hip arthroscopy. Patients must also have access to a smartphone device in order to utilize the SAGA BFR application for use. The application is free to use.\n\nExclusion Criteria:\n\n* bilateral hip surgeries to be performed within 12 weeks of each other, concomitant Peri-acetabular osteotomy, soft tissue repairs (hamstring, glute repairs), clinically diagnosed hip dysplasia, and the following BFR contraindications:\n\n  * Deep Vein Thrombosis (DVT)\n  * Pulmonary Embolism\n  * Hemorrhagic\u002FThrombolytic Stroke\n  * Clotting Disorders\n  * Hemophilia or taking blood thinners\n  * Pregnant or up to 6 months post-partum\n  * Untreated Hypertension\n  * Untreated Hypotension\n  * Rhabdomyolysis or recent traumatic injury","60 Years",{"count":212,"type":18},120,[72],"The investigators plan to investigate the efficacy of blood flow restriction (BFR) therapy in post operative rehabilitation following hip arthroscopy. BFR has shown to be great at helping the recovery process. SAGA is a well-known smart training technology company, and the investigators aim to partner with SAGA to use the BFR cuffs as the intervention method. The BFR cuff will be added to the current SOC for hip scope PT for the intervention group.",[26],"2024-12-06",{"date":218,"type":50},"2024-12-11",{"date":220,"type":50},"2022-04-29",{"date":222,"type":18},"2025-12-31",{"name":224,"class":57},"University of Colorado, Denver",{"id":226,"slug":4,"hasResults":10,"nctId":227,"briefTitle":228,"officialTitle":229,"acronym":4,"eligibilityCriteria":230,"healthyVolunteers":10,"sex":15,"minAge":66,"maxAge":210,"enrollmentInfo":231,"targetDuration":4,"studyType":70,"phases":233,"briefSummary":234,"conditions":235,"keywords":238,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":243,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":249,"locationsCount":58},"100538287","NCT06288867","A 12 Months Prospective Study Comparing Functional Outcome Scores in Hip Arthroscopic Labral Repair Versus Debridement","Arthroscopic Labral Repair Versus Debridement In Hip Labral Tears: A Prospective Comparative Study","Inclusion Criteria:\n\n* Sex: both sexes.\n* Age: 18 years - 60 years.\n* Femoroacetabular impingement (FAI) including all types (cam, pincer, and combined).\n* Traumatic Labral tears\n\nExclusion Criteria:\n\n* Previous hip surgery.\n* Hip joint dysplasia, defined by both center edge (CE) angles \\\u003C25 degrees and Acetabular Index angle \\>10 degrees.\n* Osteoarthritis grade \\>2 according to Tönnis classification.",{"count":232,"type":18},20,[72],"This study aims to address hip labral tears and compare between arthroscopic labral repair versus debridement.",[26,236,237],"Acetabular Labral Tear","Femoro Acetabular Impingement",[239,240,241,236],"Hip Arthroscopy","Labral Repair","Labral Debridement","2024-08-26",{"date":244,"type":50},"2024-08-27",{"date":246,"type":50},"2024-08-01",{"date":248,"type":18},"2025-12-01",{"name":250,"class":57},"Ain Shams University",""]