Status:

COMPLETED

Induction of Labor in Pregnant Women With Prelabor Rupture of Membranes - Oxytocin or Misoprostol

Lead Sponsor:

Ain Shams Maternity Hospital

Conditions:

Prelabor Rupture of Membranes

Eligibility:

FEMALE

18-40 years

Phase:

PHASE4

Brief Summary

The aim of study is to compare the efficacy and safety of oral misoprostol versus oxytocin in induction of labor in pregnant women with prelabor rupture of membranes at term.

Detailed Description

Type of Study: Randomized controlled clinical trial. Study Setting: The study will be conducted at Ain Shams University Maternity Hospital (ASUMH) at labor ward. Study Population: pregnant women atte...

Eligibility Criteria

Inclusion

  • Gestational age (36-42 weeks).
  • Prelabor rupture of membranes within the last 24hours
  • Vertex presentation

Exclusion

  • History of medical diseases (HTN, diabetes milletus, systemic lupus erythematosus, cardiac, etc.).
  • Antepartum hemorrhage
  • Chorioamnionitis / prelabor rupture of membranes \>24hours
  • Multiple pregnancy.
  • Abnormal fetal heart rate pattern upon admission
  • Intrauterine growth restriction
  • Fetal malpresentation.
  • Previous uterine scar.
  • Estimated fetal weight more than 4kg.
  • Patients already in labor
  • Contraindication for prostaglandin/oxytocin use (allergy,..)

Key Trial Info

Start Date :

February 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 16 2022

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT05215873

Start Date

February 1 2021

End Date

May 16 2022

Last Update

June 23 2022

Active Locations (1)

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1

Ain Shams Maternity Hospital

Cairo, Egypt