MedPath

The effect of progesterone in patients with premature rupture of membranes

Not Applicable
Conditions
Premature rupture of membranes, labour delayed by therapy.
Premature rupture of membranes, labour delayed by therapy
Registration Number
IRCT201512077676N4
Lead Sponsor
Vice Chancellor for Research and Technology University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

pregnant women with gestational age between 26 to 32 weeks with premature rupture of membranes (PROM); signing informed consent.
Exclusion criteria: fetal abnormalities; genetic abnormalities that can affect fetal growth that have been checked by ultrasound at 18 to 20 weeks and 28 to 32 weeks. Along with trisomy screening marker with double or quad marker; precambrian patients; chronic high blood pressure; overt diabetes; pregnancy-related diabetes; detachment; prolapsed umbilical cord; chorioamnionitis; gestational age over 32 weeks (because there isn’t sufficient time to study the effects of progesterone); patient who have had a rupture of the membranes after 36 hours; patient who are in active phase.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
engthening the interval between the pre-term delivery runny. Timepoint: Daily. Method of measurement: Physical examination.
Secondary Outcome Measures
NameTimeMethod
Improving Perinatal Outcomes. Timepoint: Follow baby daily until discharge. Method of measurement: Physical examination.
© Copyright 2025. All Rights Reserved by MedPath