Treatment of postoperative pain with intravenous ketorolac in mandibular fracture surgery
Phase 2
- Conditions
- Acute pain.Acute pain
- Registration Number
- IRCT201607271674N13
- Lead Sponsor
- Vice-Chancellery of Research and Technology, Shiraz University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Inclusion criteria included 16-47 year old patients whom were scheduled to undergo mandibular fractured surgy; Subjects who had systemic disease and history of drug consumption; history of drug allergic reaction; hepatic and renal dysfunction and lack of signed informed consent will be excluded from the study sample
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of postoperative pain. Timepoint: Immediately after surgery to 4 hours after surgery each 5 min. Method of measurement: VAS.;Use of narcotic (Pethedin) after surgery for postop. pain management. Timepoint: To 4 hours after surgery. Method of measurement: Nursing reports.
- Secondary Outcome Measures
Name Time Method Post-operative complications of Ketoroloc. Timepoint: Immediately after surgery to 4 hours after surgery. Method of measurement: Nursing reports.