sing of short leg splint for immobilizatio
Not Applicable
Recruiting
- Conditions
- ower limb soft tissue injuries.
- Registration Number
- IRCT20170105031787N2
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
Patients, who admitted in the emergency department of 7tir Hospital” in Tehran with a complaint of lower limb trauma and need splinting
Exclusion Criteria
Patients under eighteen years old and those that can not be follow up will be rolled out. Patients who had long bone fracture Patients who had lower limb rupture Patients who had dislocation Patients who had laceration needs to repair
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Recovery time. Timepoint: every week from splinting to removal time. Method of measurement: telephone or in-person interviews with patients.;Swelling. Timepoint: Before intervention; one week after intervention; two weeks after intervention; three weeks after intervention. Method of measurement: telephone or in-person interviews with patients.;Pain. Timepoint: every week until 3 weeks from splinting. Method of measurement: telephone or in-person interviews with patients according to pain score.;Complication such as compartment syndrome, burning of skin or sore. Timepoint: every week from splinting to removal time. Method of measurement: telephone or in-person interviews with patients.;Tolerance. Timepoint: every week from splinting to removal time. Method of measurement: telephone or in-person interviews with patients.
- Secondary Outcome Measures
Name Time Method