Comparison of Apotel (paracetamol) & ketorolac on post operative pain relief following elective lower abdominal surgery
Phase 2
- Conditions
- lower abdomen surgeries.Pain localized to other parts of lower abdomen
- Registration Number
- IRCT2015081723663N1
- Lead Sponsor
- Vice Chancellor for Research, Bandar Abbas University of Medical Sc
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 320
Inclusion Criteria
Inclusion Criteria;
ASA I-II; patients undergoing elective lower abdomen surgeries.
Exclusion Criteria;
Opium addicted patients; drug allergy history; a history of gastrointestinal bleeding or kidney failure; lack of consent to participate in this study
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: At 0 ,2,6,24 hours after surgery. Method of measurement: (VAS) Visual Analogue Scale.;Postoperative pain. Timepoint: At 0,6,12,24 hours after surgery. Method of measurement: (BSAS) Bedside Shivering Assessment Scale.
- Secondary Outcome Measures
Name Time Method