Analgesic effect of paracetamol and meperidine after cesarean section.
Phase 3
- Conditions
- Cesarean delivery.Single delivery by caesarean section
- Registration Number
- IRCT201405262624N17
- Lead Sponsor
- Vice chancellor for research ,Iran University of Medical Sciences.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
all patients after cesarean section with normal body mass index( between 18.5 and 25).
Exclusion criteria: Drug abuse; history of allergy to paracetamol or mepiridine; history of hepatitis; renal failure; heart failure; respiratory disease;CNS disorders; coagulopathy; sedative use; psychiatric disorders and complication of cesarean section.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain . Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: VAS.
- Secondary Outcome Measures
Name Time Method eed to more analgesic. Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: questionair.;Paracetamol adverse effects. Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: VAS.;Side effects of meperidine. Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: VAS.