Efficacy of bone reduction device in femoral fracture reductio
Phase 3
- Conditions
- femoral shaft fracture.Fracture of shaft of femurS72.3
- Registration Number
- IRCT20230219057449N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 48
Inclusion Criteria
adult patient aged 20
fracture type OTA-A3
closed femur fracture
one week interval between trauma to surgery
consent form
Exclusion Criteria
pathologic fracture
other fracture or trauma affecting rehabilitation program
unconsciousness affecting rehabilitation program
concomitant systemic disease affecting union such as diabetes or malignancy
drug abuse, smoking or addictin
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method nion rate. Timepoint: months 1, 2, 3 and 6. Method of measurement: radiographic union that verified with three of four bridging callus in medial, lateral, anterior and posterior cortexes in radiographic images.
- Secondary Outcome Measures
Name Time Method Surgery time. Timepoint: skin incision to final suture. Method of measurement: chromometer.;Fluoroscopy time. Timepoint: from start to ending of surgery. Method of measurement: chronometer.;Blood loss. Timepoint: the day after surgery. Method of measurement: hematocrit decrease.;Infection. Timepoint: each week in first month after surgery. Method of measurement: superficial or deep discharge or systemic symptoms.