Evaluation oral potassium diclofenac effectiveness in pain control of patients with isolated and acute limb trauma
Not Applicable
- Conditions
- Condition 1: lower limb trauma. Condition 2: upper limb trauma. Condition 3: wrist and hand trauma. Condition 4: elbow and shoulder trauma. Condition 5: pelvic and thigh trauma. Condition 6: foot trauma.s92-0s62-0s42-0s72-0s80-s89s50-59s60-69s40-49s70-79
- Registration Number
- IRCT201703018872N11
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 54
Inclusion Criteria
Inclusion Criteria: isolated and closed limb trauma; age>18; pain score> 3( pain score) ;consent to participation in the study.
Exclusion Criteria
cardiovascular instability; recent analgesic consumption; drug addiction; intravenous opioid administration by prehospital emergency staff or triage nurse; oral intake intolerance; decreased level of consciousness; dementia; multiple trauma, open limb fractures; language barrier.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of pain severity. Timepoint: before intervention and then 5, 15, 30, 60 min and 4 hour after intervention. Method of measurement: VAS.
- Secondary Outcome Measures
Name Time Method Patient satisfaction. Timepoint: after completion on intervention. Method of measurement: patient claim.