[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hip-joint\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hip-joint":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,75],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100633386","comparative-effects-of-post-isometric-relaxation-versus-active-isolated-stretch-in-patients-with-piriformis-syndrome-100633386",false,"NCT07526012","Comparative Effects Of Post Isometric Relaxation Versus Active Isolated Stretch In Patients With Piriformis Syndrome","Inclusion Criteria:\n\n* Age between 20-55 years\n* Both genders\n* Buttock pain that may radiates to posterior thigh but not beyond the knee\n* Pain aggravated by sitting, climbing stairs or hip rotation.\n* Tenderness upon palpation over the sciatic foramen.\n* Positive FAIR test.\n\nExclusion Criteria:\n\n* Malignancies\n* History of steroid therapy over 3 months\n* Rheumatoid arthritis or osteoarthritis\n* Avascular necrosis of the femoral head\n* Osteoporosis\n* Fracture of the femur\n* Hip deformity","ALL","20 Years","55 Years",{"count":19,"type":20},40,"ESTIMATED","INTERVENTIONAL",[23],"NA","The purpose of this study is to evaluate the comparative effects of post-isometric relaxation (PIR) and active isolated stretch (AIS) techniques on reducing pain, improving range of motion, and decreasing functional disability in individuals with piriformis syndrome. A total of 40 participants will be recruited, aged 20-55 yrs, with confirmed piriformis syndrome. Participants will be randomized into two equal groups. Group A (post isometric relaxation) and Group B (active isolated stretch). Both groups will receive Conventional Therapy (Thermotherapy, Electrotherapy).\n\nStudy variables include:\n\n* Independent Variable: Post Isometric Relaxation and Active Isolated Stretching.\n* Dependent Variables: Pain (measured by Visual Analog Scale), Functional Disability (assessed via Oswestry Disability Index), Range of Motion (assessed via Goniometer).\n* Control Variables: Age, Gender, BMI, Baseline Pain\u002F Disability Scores\u002FROM\n\nThe intervention will last 2 weeks with 6 sessions (3 sessions per week). Assessments will be conducted at baseline (Week 1, Pre-treatment) and Post every second session. Data will be analyzed to compare immediate and short-term effects of the two interventions.\n\nThis study aims to provide evidence for targeted manual therapy approaches in priformis syndrome, potentially guiding clinicians toward the most effective technique for pain reduction, improve ROM and decrease functional disability.",[26,27,28],"Piriformis Syndrome","Low Back Pain","Hip Joint","RECRUITING","2026-05-18",{"date":32,"type":33},"2026-05-20","ACTUAL",{"date":32,"type":20},{"date":36,"type":20},"2026-07-15",{"name":38,"class":39},"Foundation University Islamabad","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":15,"minAge":49,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":61,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":74},"100620637","muscle-damage-of-the-tfl-tensor-fascia-latae-during-total-hip-arthroplasty-tha-through-direct-anterior-approach-daa-100620637","NCT07360210","Muscle Damage of the TFL (Tensor Fascia Latae) During Total Hip Arthroplasty (THA) Through Direct Anterior Approach (DAA)","Muscle Damage of the TFL (Tensor Fascia Latae) During Total Hip Arthroplasty (THA) Through Direct Anterior Approach (DAA), Evaluation of the Correlation With Short Term Functional Results","TFL","Inclusion Criteria:\n\n* adult (\\>18 years old),\n* patient undergoing primary Total Hip Arthroplasty through Direct Anterior Approach for osteoarthritis\n\nExclusion Criteria:\n\n* hip dysplasia\n* leg length discrepancy greater than 2cm\n* history of homolateral hip surgery\n* neuromuscular pathology\n* patients declining the protocol","18 Years",{"count":51,"type":20},150,[23],"Direct Anterior Approach (DAA) is known to cause damage to the TFL during the surgical approach, the point of this study is to evaluate the impact between the severity of the per operative TFL damage and the functional short term results.",[28,55,56,57,58,59,60],"Surgery","Arthroplasty","Replacement","Surgical Wound","Muscle Injury","Fascia Lata",[62,63],"TFL damage","Total Hip Arthroplasty through Direct Anterior Approach","NOT_YET_RECRUITING","2026-01-14",{"date":67,"type":33},"2026-01-22",{"date":69,"type":20},"2026-02",{"date":71,"type":20},"2026-10",{"name":73,"class":39},"University Hospital, Bordeaux",2,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":15,"minAge":82,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":21,"phases":85,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":40},"100511456","effects-of-flumazenil-on-recovery-after-total-intravenous-anesthesia-with-remimazolam-100511456","NCT05939674","Effects of Flumazenil on Recovery After Total Intravenous Anesthesia With Remimazolam","Effects of Flumazenil on Recovery After Total Intravenous Anesthesia With Remimazolam in Elderly Patients Undergoing Hip Joint Surgery: a Prospective Randomized Controlled Study.","Inclusion Criteria:\n\n* Patients over 65 years old scheduled for hip joint surgery\n\nExclusion Criteria:\n\n* Patients with impaired consciousness or delirium before surgery\n* Patients who are hemodynamically unstable before surgery\n* Patients with a history of neurological or neuromuscular disorders or use of medications that affect neurological or neuromuscular function\n* Patients who have taken sedatives (anti-anxiety medications, antipsychotics, antidepressants, sleep aids) within the past 24 hours\n* Patients with known allergy to benzodiazepine, flumazenil\n* Patients with galactose intolerance, Lapp lactase deficiency, glucose-galactose malabsorption\n* Patients with hypersensitivity to Dextran40\n* Patients who have been taking benzodiazepine for long term\n* Patients with end stage renal disease requiring hemodialysis\n* Patients with history of acute angle glaucoma\n* Patients with alcohol or substance dependence\n* ASA classification 4 or 5","65 Years",{"count":84,"type":20},24,[23],"Remimazolam is a medication that has the advantage of a short half-life and reversibility with flumazenil. In clinical situations, the use of flumazenil for the reversal of sedation is common, but there is no precise indication for its administration. In this study, we aim to investigate the necessity of routine flumazenil use after administering remimazolam for intravenous anesthesia.",[88,89,28,90],"Flumazenil Adverse Reaction","Remimazolam","Elderly Patients","2025-09-07",{"date":93,"type":33},"2025-09-12",{"date":95,"type":33},"2023-09-19",{"date":97,"type":20},"2026-06",{"name":99,"class":39},"Pusan National University Yangsan Hospital"]