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Evaluation of Efficacy of Two Therapeutic Strategies for Cervical Maturation Before Medical Termination

NCT03194126 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2023-10-03

No results posted yet for this study

Summary

Reducing the time patients spend in the labor and delivery room saves money and reduces patient discomfort as well and reducing complications. We will compare two methods for inducing cervical maturation in order to shorten the time taken between administration of drugs and delivery.

Conditions

  • Medical; Abortion, Fetus

Interventions

PROCEDURE

Mifepristone + Misoprostol OR oxytocine + laminaria

Three laminaria placed 12 hours prior to administration of misoprostol

PROCEDURE

Mifepristone + Misoprostol OR oxytocine

standart support

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Nīmes

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-11
Primary Completion
2023-09-25
Completion
2023-09-25

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 NCT03194126 on ClinicalTrials.gov