Clinical Trials Directory

Trials / Completed

CompletedNCT00410345

Cervical Rippening With Antiprogesterone in Midtrimester Abortions

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
145 (actual)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Induction of midtrimester abortion includes cervical ripening and then contraction to induce uterine evacuation. There are several protocols, but most of them include using prostaglandins (PG). The disadvantages of using PG include uncomfortable side effects and limits of using it for women after cesarean section. Mifepristone is an antiprogesterone drug and been used for induction of abortion in first and second trimesters abortions. The aim of this study is to explore the effectiveness of Mifepristone for cervical ripening before high dose Oxytocin drip.

Detailed description

The aim of this study is to explore the effectiveness of Mifepristone for cervical ripening before high dose Oxytocin drip in midtrimester abortions. After informed consent, all the women will be randomized for Mifepristone or placebo. 48 hours later, high dose oxytocin drip will be started and we will examine the success rate to induce abortion, the duration from starting oxytocin till evacuation of uterus and side effects.

Conditions

Interventions

TypeNameDescription
DRUGMifepristone

Timeline

Start date
2004-08-01
Primary completion
2008-05-01
Completion
2008-05-01
First posted
2006-12-12
Last updated
2017-03-01

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00410345. Inclusion in this directory is not an endorsement.