Comparison the effectiveness of burn drugs on controlling pain of burn patients
Phase 2
- Conditions
- burn.Burn and corrosion
- Registration Number
- IRCT201605171310N10
- Lead Sponsor
- Vice chancellor for research, Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
age between 18 and 60 years; Burn with grade 2 and 3, burns 20 percent to 50 percent; AS A Class 1 and 2
Exclusion criteria: pregnant women; People with any known chronic mental illness; Patients with history of chronic underlying cardiac, lung and kidney disease; patients treated with certain medications such as immunosuppressive medications or chemotherapy or Corticosteroid
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of pain. Timepoint: Beginning of the study, half an hour, an hour, two hours, four hours, six hours after start of surgery. Method of measurement: Using visual analogue scale (VAS).
- Secondary Outcome Measures
Name Time Method