Postoperative analgesic effect of tramadol and bupivacaine for cesarean sectio
Not Applicable
- Conditions
- cesarean section.Delivery by elective caesarean section
- Registration Number
- IRCT201106203468N8
- Lead Sponsor
- Pain Research Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
complete health condition; first or second time elective cesarean section candidate; age between 18-45 years.
Exclusion criteria: sensitivity to study drugs; opium addiction
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: 1,2,3 hours after cesarean. Method of measurement: visual analogue scale.;Time to first analgesic request. Timepoint: time between intervention and first analgesic administratin. Method of measurement: minutes.;Total analgesic consumption. Timepoint: 24 after intervention. Method of measurement: mg/kg consumped meperidine.
- Secondary Outcome Measures
Name Time Method Side effects. Timepoint: 24 hours after intervention. Method of measurement: observation.