Comparison of sublingual buprenorphine and intravenous fentanyl pump for cesarean section pain control
Not Applicable
Recruiting
- Conditions
- caesarean section.Delivery by elective caesarean section
- Registration Number
- IRCT2017081723559N14
- Lead Sponsor
- Vice chancellor for research, Ardabil University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Patients with spinal anesthesia during cesarean section. Exclusion criteria: History of drug abuse.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Four times (2,6,12and 24 hours) after intervention. Method of measurement: Visual analog scale.
- Secondary Outcome Measures
Name Time Method Vomiting. Timepoint: Up to 24 hours after intervention. Method of measurement: Clinical.