[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"femur-fractures\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:femur-fractures":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100649807","robot-assisted-closed-reduction-and-internal-fixation-for-femoral-shaft-fractures-100649807",false,"NCT07738380","Robot-Assisted Closed Reduction and Internal Fixation for Femoral Shaft Fractures","Robot-Assisted Versus Traditional Closed Reduction and Internal Fixation for Femoral Shaft Fractures: A Randomized Controlled Trial","Inclusion Criteria：\n\n* Age 18 to 80 years, inclusive.\n* Unilateral, acute, closed femoral shaft fracture.\n* AO\u002FOTA classification 32-A, 32-B, or 32-C femoral shaft fracture.\n* Time from injury to surgery no more than 21 days.\n* Ability to walk independently before injury, with or without assistive devices.\n* Ability to provide written informed consent.\n\nExclusion Criteria：\n\n* Open fracture.\n* Multiple severe trauma requiring immediate priority management.\n* Asymmetry of the lower limbs.\n* History of ipsilateral femoral shaft malunion.\n* History of ipsilateral femoral deformity that significantly affects assessment of - limb rotation or length.\n* Ipsilateral fracture at another site.\n* Pathological fracture caused by tumor, metabolic bone disease, or other underlying bone pathology.\n* Complex hardware from previous ipsilateral surgery.\n* History of ipsilateral surgery that significantly affects clinical or radiographic evaluation.\n* Active infection.\n* Severe underlying medical condition that makes the patient unable to tolerate surgery.\n* Cognitive impairment that prevents study participation or follow-up.\n* Poor compliance with study procedures or follow-up.\n* Pregnancy or lactation.\n* Judged by the investigators to be unsuitable for enrollment.\n* Unable to complete the planned follow-up period.\n* Refusal to undergo randomization.\n* Refusal to participate in the clinical study.","ALL","18 Years","80 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to evaluate the safety and efficacy of robot-assisted closed reduction for patients with femoral shaft fractures. The main questions it aims to answer are:\n\nDoes robot-assisted closed reduction provide a statistically significant improvement in the excellent and good reduction rates compared to conventional surgeon-performed reduction? How do the two reduction methods compare in terms of surgical efficiency, fracture healing, and patient functional outcomes? Researchers will compare the robot-assisted closed reduction group to the conventional surgeon-performed reduction group to see if robot-assisted surgery improves the precision of fracture reduction, stability of alignment, and post-operative functional recovery while minimizing trauma.\n\nParticipants will:\n\nUndergo standardized screening to ensure they meet the inclusion criteria for acute, unilateral, closed femoral shaft fractures (Arbeitsgemeinschaft für Osteosynthesefragen\u002FOrthopaedic Trauma Association \\[AO\u002FOTA\\] classification 32).\n\nBe randomized in a 1:1 ratio to receive either robot-assisted closed reduction or traditional surgeon-performed closed reduction, both followed by internal fixation.\n\nComplete standardized perioperative management and follow-up assessments at 1, 3, 6, and 12 months post-surgery, including functional scales such as the Lower Extremity Functional Scale (LEFS) and the EuroQol Five-Dimensional Five-Level questionnaire (EQ-5D-5L), as well as radiographic imaging to monitor bone healing and potential complications.",[27,28,29],"Femoral Shaft Fractures","Femur Fractures","Femur Fracture","RECRUITING","2026-07-28",{"date":33,"type":34},"2026-07-31","ACTUAL",{"date":36,"type":34},"2026-07-01",{"date":38,"type":21},"2028-12-29",{"name":40,"class":41},"Beijing Jishuitan Hospital","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":4,"enrollmentInfo":52,"targetDuration":54,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":42},"100618471","predicting-of-frailty-100618471","NCT07332052","Predicting of Frailty","Comparison of Parameters That Can be Used to Predict Frailty in Elderly Femur Fracture Patients.","PRE-FRAIL","Inclusion Criteria:\n\n* Patients aged 65 years and older.\n* Confirmed diagnosis of trochanteric femur fracture.\n* Planned for orthopedic surgery under general or regional anesthesia.\n* Ability to provide written informed consent (either by the patient or a legal representative).\n\nExclusion Criteria:\n\n* Patients with advanced dementia or severe cognitive impairment who cannot cooperate with the handgrip strength test or Fried criteria questionnaire.\n* Patients with terminal-stage diseases or those under palliative care.\n* History of neuromuscular diseases or severe muscle-wasting conditions that affect the lower limbs (e.g., advanced muscular dystrophy).\n* Patients with active infections or skin lesions at the site of ultrasound measurement (rectus femoris area).\n* Emergency cases requiring immediate surgery where preoperative assessment cannot be completed.","65 Years",{"count":53,"type":21},100,"1 Day","OBSERVATIONAL","This study aims to evaluate the frailty status of elderly patients undergoing surgery for hip fractures (femur trochanteric fractures). Since frailty is a critical factor in surgical outcomes and recovery, researchers want to find simple, fast, and objective ways to measure it. This study will investigate muscle thickness measured by ultrasound, handgrip strength measured by a dynamometer, and routine blood test values can accurately predict a patient's frailty level. If these objective methods are proven effective, it will help anesthesia and surgical teams manage the perioperative process more safely for high-risk elderly patients",[28,58,59],"Frailty","Sarcopenia",[61,58,62,59,63],"Geriatric Anesthesia","Hip Fracture","Rectus Femoris","NOT_YET_RECRUITING","2025-12-30",{"date":67,"type":34},"2026-01-12",{"date":69,"type":21},"2026-01-20",{"date":71,"type":21},"2026-08-15",{"name":73,"class":41},"ali ihsan uysal"]