Clinical Trials Directory

Trials / Unknown

UnknownNCT00920465

Treatment Regimens for Mifegyne and Cytotec

Comparison of the Effectiveness of Abortive Measures From the Administration of Mifegyne and Cytotec at One and Two Visits

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Western Galilee Hospital-Nahariya · Other Government
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test two regimens of mifegyne and cytotec for medical abortion. The investigators hypothesize that administration of both medications during one hospital visit will not compromise effectiveness.

Conditions

Interventions

TypeNameDescription
DRUGmifegyne and cytotecOne day dosage versus two days dosage

Timeline

Start date
2009-06-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2009-06-15
Last updated
2011-05-25

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00920465. Inclusion in this directory is not an endorsement.

Treatment Regimens for Mifegyne and Cytotec (NCT00920465) · Clinical Trials Directory