Comparison of expectant treatment outcomes in pregnant women with preterm premature rupture of membranes (PPROM) at home and hospital

Early Phase 1

Conditions: preterm premature rupture of membranes.
Premature rupture of membranes

Registration Number: IRCT20181115041666N1

Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: Female

Target Recruitment: 100

Inclusion Criteria

alive singleton pregnancy
Gestational age between 25 and 34 weeks
The absence of chorioamnionitis symptoms
The lack of evidence for fetal distress
No vaginal bleeding
Patient's consent
Evaluation for 72 hours in hospital
Cephalic presentation
Having a caretaker at home
Taking 60 minutes at most to reach the first treatment center
The diameter of maximum vertical pocket of the amniotic fluid is more than 2 Cm²

Exclusion Criteria

Occurrence of chorioamnionitis
disturbed fetal tests of health evaluation
Vaginal bleeding
Patient's unwillingness to continue participation in the study
Gestational age of less than 25 weeks of labor (greater than 3 cm of dilatation)

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of expectant treatment course. Timepoint: From hospitalization to delivery. Method of measurement: duration in days.;Gestational age at the time of delivery. Timepoint: at the time of birth. Method of measurement: Course duration is measured based on the number of weeks.;Birth weight. Timepoint: at the time of child birth. Method of measurement: using scales.;Number of cesarean section. Timepoint: Time of birth. Method of measurement: number of cesarean section in each group.

Secondary Outcome Measures