IRCT20180708040381N3CompletedPhase 3
Comparison of intravenous acetaminophen effect with 24-hour and routine drip on control of pain in patients undergoing cesarean section
Azad Islamic University, Najaf Abad Branch0 sites80 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 80
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 16 years to 40 years (—)
- Sex
- Female
Inclusion Criteria
- •Women aged 16 to 40 years
- •Candidate for cesarean section
- •No smoke and opioids consumption
- •ASA class 1 or 2
Exclusion Criteria
- •Allergy to any of the drugs used in study
- •Liver disease
- •History of seizure
Investigators
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