[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100628186":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":26,"locations":31,"responsibleParty":49,"collaborators":26,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":26,"eligibilityCriteria":58,"healthyVolunteers":54,"sex":59,"minAge":60,"maxAge":26,"enrollmentInfo":61,"targetDuration":26,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":26,"overallStatus":34,"whyStopped":26,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Konya Meram State Hospital","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"FRONT Block Group","EXPERIMENTAL","Participants in this group will receive an ultrasound-guided unilateral Femoral Rami and Obturator Nerve Trunk (FRONT) block in addition to standardized multimodal postoperative analgesia.",[13,14],"Procedure: FRONT Block (Femoral Rami and Obturator Nerve Trunk Block)","Procedure: Standard Multimodal Analgesia",{"label":16,"type":17,"description":18,"interventionNames":19},"Control Group","ACTIVE_COMPARATOR","Participants in this group will receive standardized multimodal postoperative analgesia without FRONT block.",[14],[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","FRONT Block (Femoral Rami and Obturator Nerve Trunk Block)","Ultrasound-guided unilateral FRONT block targeting the femoral rami and obturator nerve trunk will be performed",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Standard Multimodal Analgesia","Standardized postoperative multimodal analgesia including intravenous paracetamol, nonsteroidal anti-inflammatory drugs, and rescue opioid analgesia as required.",[16,9],[32],{"facility":33,"status":34,"city":35,"state":26,"zip":36,"country":37,"countryCode":26,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Betul Kozanhan","RECRUITING","Konya","42005","Turkey (Türkiye)",{"type":39,"coordinates":40},"Point",[41,42],32.48464,37.87135,{"lat":42,"lon":41},[45],{"name":33,"role":46,"phone":47,"phoneExt":26,"email":48},"CONTACT","(0332) 310 50 00","betulkozanhan@gmail.com",{"type":50,"investigatorFullName":33,"investigatorTitle":51,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Prof. Dr.","100628186","front-block-for-quality-of-recovery-after-total-hip-arthroplasty-100628186",false,"NCT07458360","FRONT Block for Quality of Recovery After Total Hip Arthroplasty","Effect of Femoral Rami and Obturator Nerve Trunk (FRONT) Block on Postoperative Quality of Recovery After Total Hip Arthroplasty: A Prospective Randomized Controlled Trial","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Scheduled for total hip arthroplasty under spinal anesthesia\n* American Society of Anesthesiologists (ASA) physical status I-III\n* Ability to understand and complete the QoR-15 questionnaire\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Refusal to participate\n* Contraindication to spinal anesthesia or regional block\n* Allergy to study medications\n* Chronic opioid use (daily use for more than 3 months)\n* Neurological or neuromuscular disorders affecting the lower extremities\n* Infection at the injection site\n* Coagulation disorders\n* Cognitive impairment prevents questionnaire completion","ALL","18 Years",{"count":62,"type":63},80,"ESTIMATED","INTERVENTIONAL",[66],"NA","This prospective randomized controlled trial evaluates the effect of ultrasound-guided unilateral Femoral Rami and Obturator Nerve Trunk (FRONT) block on postoperative quality of recovery in patients undergoing elective total hip arthroplasty.",[69,70,71],"Osteoarthritis of the Hip","Postoperative Pain","Quality of Recovery","2026-04-25",{"date":74,"type":75},"2026-04-28","ACTUAL",{"date":72,"type":75},{"date":78,"type":63},"2026-07-05",{"name":5,"class":6},1]