Comparison of the effect pethidine, paracetamol and their combination on the reduction of labor pain and the level of satisfaction of primiparous wome
Phase 3
Recruiting
- Conditions
- abor pain.Maternal distress during labor and deliveryO75.0
- Registration Number
- IRCT20120215009014N455
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 111
Inclusion Criteria
Age of 18 to 40 years
Term pregnancy
A singleton with a cephalic display
Cervical dilatation 4 cm
Pregnant women undergoing induction of labor with oxytocin
Exclusion Criteria
Analgesic consumption in the last 24 hours
Preeclampsia and eclampsia
Severe obesity
Intrauterine fetal death
Fetal abnormalities
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method abor pain intensity. Timepoint: In the first and fifth minutes after delivery. Method of measurement: Using visual analog scale (VAS).;The level of satisfaction. Timepoint: After the third stage of labor. Method of measurement: Using McKay's satisfaction questionnaire.
- Secondary Outcome Measures
Name Time Method Side effects (nausea, vomiting, maternal tachycardia, respiratory depression, drowsiness, itching). Timepoint: In the first, second and third stage of labor. Method of measurement: With clinical examination and history taking.