Comparison of the effect of promethazine and topical magnesium sulfate on labor pain severity and progression in primiparous wome

Phase 2

Recruiting

• Conditions: Delivery.; Spontaneous vertex delivery; O80.0

• Registration Number: IRCT20160427027633N10
• Lead Sponsor: Kermanshah University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 24 June 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

Willingness to participate in the study
Age between 18 and 35 years
Full-term pregnancy
Primiparous
Single and live fetus with cephalic presentation
Estimated fetal weight between 2500 and 4000 grams
Low-risk pregnancy
No use of narcotic drugs and painkillers during In the past 48 hours
The absence of chronic and systemic diseases such as diabetes, hypertension, heart disease, epilepsy
The beginning of the active phase (3-4 cm cervical dilatation)
No rupture of membrane

Exclusion Criteria

Withdrawal of participants during the study
The occurrence of any obstetric emergencies
Contraindications of normal delivery such as: fetal distress, placental abruption, severe vaginal bleeding, umbilical cord prolapse, etc.
The occurrence of emergency cesarean section before the completion of the study
Non-cooperation of participants

Study & Design

• Study Type: interventional
• Study Design: Not specified