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Enrolling by invitation

NCT Number: NCT07802041

Planned Early Induction of Labor vs Expectant Management for PROM

The goal of this randomized controlled trial is to compare planned early induction of labor with expectant management in women with term premature rupture of membranes (PROM) at 37-42 weeks of gestation. The main questions it aims to answer are:

Does planned early induction of labor reduce maternal and fetal complications compared with expectant management? Is there a difference in the frequency of cesarean section, chorioamnionitis, and fetal distress between the two management strategies? Researchers will compare active management (induction of labor within 24 hours) with expectant management (observation for 24 hours while awaiting spontaneous onset of labor).

Participants will:

Be women aged 18-45 years with singleton pregnancies and PROM at 37-42 weeks. Be randomly assigned to either active or expectant management. Receive routine monitoring and intravenous antibiotics until delivery. Be followed until delivery, with maternal and fetal outcomes recorded.

Enrolling by invitation

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Pakistan institute of medical sciences Islamabad

Islamabad, Pakistan

About this study

This randomized controlled trial will compare planned early induction of labor (active management) with expectant management in women with term premature rupture of membranes (PROM).

PROM is defined as rupture of the fetal membranes before the onset of labor. At term, the optimal timing of delivery remains an important clinical consideration because prolonged rupture of membranes may increase the risk of maternal and neonatal infection, while early delivery may increase interventions such as induction of labor and cesarean section.

The study will be conducted in the Department of Obstetrics and Gynaecology, PIMS Hospital, Islamabad, over a period of six months after approval of the synopsis. A total of 734 women will be enrolled using consecutive sampling and randomly allocated into two equal groups of 367 participants each.

Group A - Active Management:

Labor will be induced within 24 hours of diagnosis of PROM. Prostaglandin E2 vaginal gel (1 mg) will be used for cervical ripening/induction, with repeat doses at 6-hour intervals when required, up to a maximum of three doses.

Group B - Expectant Management:

Participants will undergo observation for 24 hours following diagnosis of PROM while awaiting spontaneous onset of labor. An endocervical swab will be collected for microscopy, culture, and sensitivity. Participants will be monitored for signs of infection and fetal compromise.

Both groups will receive intravenous antibiotics according to the study protocol (ceftriaxone 1 g every 24 hours and metronidazole 500 mg every 8 hours until delivery) and will be followed until delivery.

The study will compare maternal and fetal outcomes between the two groups, particularly:

Cesarean section Chorioamnionitis Fetal distress Baseline demographic and clinical characteristics, including age, gestational age, parity, BMI, socioeconomic status, educational level, and residential status, will also be recorded.

The purpose of the study is to determine whether planned early induction of labor or expectant management is associated with better maternal and fetal outcomes in women with term PROM.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women age 18 to 45 years
  • Singleton pregnancy on ultrasound
  • Gestational age 37 to 42 weeks on LMP
  • Any parity
  • Premature rupture of membrane as per operational definition

Exclusion criteria

  • H/o active infection.
  • H/o placental abruption
  • H/o preeclampsia
  • Fetal anomalies on ultrasound

Treatment and study plan

Induction of labor with PGE2

Procedure

Induction of labor within 24 hours of diagnosis of term PROM, using prostaglandin E2 vaginal gel as per study protocol.

Expectant management

Behavioral

Observation for 24 hours while awaiting spontaneous onset of labor, with maternal and fetal monitoring.

Primary outcomes

  1. Cesearan section rate

    Time frame: From randomization until delivery

    Proportion of participants who undergo cesarean delivery in the active management group compared with the expectant management group.

  2. Chorioamnionitis

    Time frame: From randomization until delivery.

    Proportion of participants developing clinical chorioamnionitis during labor or before delivery.

  3. Fetal distress

    Time frame: From randomization until delivery.

    Proportion of participants developing fetal distress during labor requiring intervention.

Sponsors and collaborators

Lead sponsor

Pakistan Institute of Medical Sciences

Other Gov

Registry information

Official study title

Planned Early Induction of Labor Versus Expectant Management for Premature Rupture of Membranes

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Sep 3, 2026
Registry last updated
Sep 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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