The analgesic effects of Oxytoci
Phase 3
Recruiting
- Conditions
- Cesarean.
- Registration Number
- IRCT20190905044705N1
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
All patients referred for cesarean section
Lack of exclusion criteria
Exclusion Criteria
History of chronic pain and analgesic use, bleeding or coagulation disorder, peptic ulcer, renal or hepatic insufficiency and asthma, uterine atony, twins, placenta previa, Placental abruption, accreta placenta
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain after cesarean section. Timepoint: Up to 24 hours after delivery. Method of measurement: Verbal Rating Scale.
- Secondary Outcome Measures
Name Time Method