Evaluating the effect of intraperitoneal injection of ondansetron during elective caesarean section on postoperative pain intensity after caesarean sectio
Phase 3
Recruiting
- Conditions
- Examining the pain level of pregnant mothers after cesarean section.
- Registration Number
- IRCT20220610055121N1
- Lead Sponsor
- Karaj University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
A candidate for cesarean delivery due to a previous cesarean section
Having a history of cesarean delivery
healthy fetus
ASA II
Age between 20-40 years
gestational age of term
Exclusion Criteria
Having an underlying disease
Emergency cesarean section
History of ondansetron allergy
Receiving painkillers or sedatives 24 hours before surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score. Timepoint: 0, 0.5, 1, 1.5, 3, 6 hours after the surgery. Method of measurement: Visual analogue scale.
- Secondary Outcome Measures
Name Time Method