Efficacy of paracetamol for pain reductio
Phase 3
Recruiting
- Conditions
- Pain localized to other parts of lower abdomen.Pain localized to other parts of lower abdomen
- Registration Number
- IRCT20181001041196N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Elective cesarean
Spinal anesthesia
Single tone pregnancy
More than 38weeks pregnancy
Exclusion Criteria
Addiction to drug
Cardiac ,hepatic,pulmonary diseases
Allergy to paracetamol
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 1 hour after ceassarean,12hour after cesarean ,18hour after cesarean and 24hour after cesarean. Method of measurement: Vas score.
- Secondary Outcome Measures
Name Time Method