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The effect of remifentanil and hot water shower on labor pai

Phase 2
Recruiting
Conditions
labor pain.
Maternal distress during labor and delivery
O75.0
Registration Number
IRCT20111001007676N6
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
118
Inclusion Criteria

primiparous
Age between 18 and 35 years
Spontaneous onset of labor pains
No internal diseases
Cephalic presentation
Fetus without anomaly

Exclusion Criteria

Gestational age below 36 weeks
Pregnant women with large fetuses according to ultrasound (weight over 4 kg)
Pregnant women who are addicted to drugs
Pregnant women with any history of allergy to remifentanil or any local anesthetic
Pregnant women with gestational hypertension (severe preeclampsia or eclampsia)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
abor pain. Timepoint: From the beginning of the intervention until the end of labor. Method of measurement: To assess the severity of the pain, a visual pain ruler will be used (Visual Analogue Scale), which will be given a score from 1 to 10. This scale will consist of a range from 1 to 10, ranging from painless to the most severe pain ever experienced.;Duration of labor. Timepoint: from 4-5 cm cervical dilation to full cervical dilatation and the delivery time. Method of measurement: Timer.;Apgar score. Timepoint: Immediately after birth. Method of measurement: Based on Apgar Scale.
Secondary Outcome Measures
NameTimeMethod
The satisfaction of the normal delivery. Timepoint: After childbirth. Method of measurement: scale ruler.
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