Comparison of acetaminophen and pethidine in labor pain reductio
Phase 2
Recruiting
- Conditions
- pregnant women.Supervision of normal pregnancy
- Registration Number
- IRCT2017100736610N1
- Lead Sponsor
- Vice Chancellor for Research, Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Term pregnancy, request for pain relief; singleton pregnancy with cephalic presentation; no growth impairment or fetal abnormalities.
Exclusion criteria: Medical history of diseases (hepatic, renal, cardiovascular, or respiratory diseases, preeclampsia, diabetes, addiction, allergy to acetaminophen and drug abuse, and G6PD deficiency); need for induction; fetal distress; history of cesarean section.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain level. Timepoint: Before and 15 min, 30 min, 1 h, 2 h, 3 h, and 4 h after intervention. Method of measurement: VAS score.
- Secondary Outcome Measures
Name Time Method