The effect of acetaminophen drip on pain after cesarean sectio
Phase 3
- Conditions
- post operative pain.
- Registration Number
- IRCT20180708040381N3
- Lead Sponsor
- Azad Islamic University, Najaf Abad Branch
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 80
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain Score. Timepoint: First 24 hr After Surgery Every 6 hr. Method of measurement: VAS Score.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie intravenous acetaminophen's analgesic efficacy in post-cesarean pain management?
How does 24-hour intravenous acetaminophen compare to standard-of-care opioids in post-cesarean pain control?
Are there specific biomarkers associated with differential response to IV acetaminophen in post-operative pain patients?
What adverse event profiles differentiate intravenous versus oral acetaminophen in post-cesarean pain trials?
What combination analgesic strategies synergize with IV acetaminophen for enhanced post-cesarean pain relief?