[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100371237":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":41,"responsibleParty":58,"collaborators":26,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":26,"eligibilityCriteria":66,"healthyVolunteers":67,"sex":68,"minAge":69,"maxAge":70,"enrollmentInfo":71,"targetDuration":26,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":26,"overallStatus":43,"whyStopped":26,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"fullName":5,"class":6},"Rush University Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","PLACEBO_COMPARATOR","The control group will receive sham BFR, in which a non-occlusive pressure is applied with the cuff. The exercises performed will be identical to the BFR group.",[13],"Behavioral: Sham BFR Rehabilitative Therapy",{"label":15,"type":16,"description":17,"interventionNames":18},"BFR Postoperative Rehabilitation","EXPERIMENTAL","The experimental group will receive BFR postoperative rehabilitation, which will involve performing a series of blood flow restriction exercises identical to the control group.",[19],"Behavioral: Blood Flow Restriction Rehabilitative Therapy",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","Blood Flow Restriction Rehabilitative Therapy","BFR cuffs placed at the proximal thigh, just inferior to the greater trochanter.\n\nInflation time not to exceed 20 minutes. One BFR session per treatment. BFR exercise dosage: 4 sets of the following repetitions 30, 15, 15, 15, 30 second rest between sets, 1 min rest between exercises.\n\nProgress exercise if pain \\\u003C2\u002F10 on VAS and RPE \\\u003C5 on 0-10 scale. (Heerey et al), and no break down in form.",[15],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Sham BFR Rehabilitative Therapy","The schedule, type of exercises, repetition ranges, and other physical therapy interventions will be the same as the BFR experimental group - however a non-occlusive pressure will be applied with the cuff in the control group.",[9],[32],{"name":33,"affiliation":5,"role":34},"Jorge Chahla, MD PhD","PRINCIPAL_INVESTIGATOR",[36],{"name":37,"role":38,"phone":39,"phoneExt":26,"email":40},"Carla M. Edwards, PhD","CONTACT","312-563-5735","carla_edwards@rush.edu",[42],{"facility":5,"status":43,"city":44,"state":45,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":55},"RECRUITING","Chicago","Illinois","60612","United States","US",{"type":50,"coordinates":51},"Point",[52,53],-87.65005,41.85003,{"lat":53,"lon":52},[56],{"name":57,"role":38,"phone":39,"phoneExt":26,"email":40},"Carla M Edwards, PhD",{"type":59,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100371237","blood-flow-restriction-following-hip-arthroscopy-100371237",false,"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,"ALL","18 Years","40 Years",{"count":72,"type":73},56,"ESTIMATED","INTERVENTIONAL",[76],"NA","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.",[79,80],"Labral Tear, Glenoid","Femoral Acetabular Impingement","2025-12-04",{"date":83,"type":84},"2025-12-05","ACTUAL",{"date":86,"type":84},"2023-08-01",{"date":88,"type":73},"2028-01",{"name":5,"class":6},1]