Comparative study of the consequences of expected treatment of premature membrane rupture in wome

Phase 2

Recruiting

• Conditions: Premature rupture of membranes.; Premature rupture of membranes, unspecified as to length of time between rupture and onset of labor, unspecified weeks of gestation; O42.90

• Registration Number: IRCT20130812014333N179
• Lead Sponsor: Kermanshah University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 50

Inclusion Criteria

Women with the final diagnosis of Preterm premature rupture of the membranes (PPROM)
Gestational age of 34 weeks, that up to 24 hours after rupture of the membranes having labor pains
Being 34 to 36 weeks old for the waiting treatment group

Exclusion Criteria

Women with monocurion multiple pregnancies; Uncertain cardiogram
Meconium contaminated amniotic fluid
Fetal major anomaly
HELLP syndrome or preeclampsia
Symptoms of intrauterine infection

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Apgar. Timepoint: The first and fifth minutes after birth. Method of measurement: Apgar test.;Duration of hospitalization of the infant in the intensive care unit (NICU). Timepoint: After discharge. Method of measurement: Based on the record.;Respiratory distress syndrome. Timepoint: After birth. Method of measurement: Clinical examination.;Sepsis. Timepoint: After birth. Method of measurement: Clinical examination.;Uterine bleeding. Timepoint: after delivery. Method of measurement: Ask the patient and the doctor observation.