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Cervical Ripening Before Induction of Labour at Term: a Randomised Comparison of Prostin vs Propess

NCT00545194 · Status: WITHDRAWN · Phase: PHASE3 · Type: INTERVENTIONAL

Last updated 2025-09-04

No results posted yet for this study

Summary

The aim of this study is to compare two different preparation

Conditions

  • Cervical Ripening
  • Labor, Induced

Interventions

DRUG

Prostaglandin E2

Sponsors & Collaborators

  • Institut National de la Santé Et de la Recherche Médicale, France

    lead OTHER_GOV

Principal Investigators

  • Franck Perrotin, MD-PhD · Tours Universiity Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-01-31
Primary Completion
2004-10-31
Completion
2004-10-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00545194 on ClinicalTrials.gov