Comparison of oxycodone and naproxen in pain control of acute soft tissue injuries
Phase 2
- Conditions
- soft tissue injuries.musculoskeletal system and connective tissue
- Registration Number
- IRCT201112208104N3
- Lead Sponsor
- Vice Chancellor of Research; Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
Inclusion criterion: patients above 18 years old with soft tissue injuries. Exclusion criteria: contraindications for opioids and NSAIDs and presence of fracture.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain control. Timepoint: 0, 30, 60 minutes after treatment. Method of measurement: Numeric Rating Scale.
- Secondary Outcome Measures
Name Time Method Presence of side effects. Timepoint: 30 and 60 minutes after treatment. Method of measurement: Patient monitoring.;Need for follow up analgesic. Timepoint: First 24 hours after discharge. Method of measurement: Telephone follow up.