CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,001 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01966874
NCT01966874N/ACompleted
CompareCT.gov

Mifepristone and Misoprostol for the Termination of Pregnancy up to 70 Days Gestation

Gynuity Health Projects·observational·Posted Oct 22, 2013·Updated Oct 22, 2013

In Brief

An observational study for Medical; Abortion, Fetus. Completed, enrolled 1,001 participants across 1 site.

Detailed Summary

The purpose of this study is to determine the efficacy and acceptability of a regimen of 200 mg mifepristone (Zacafemyl), followed 24-48 hours later by 800 mcg of buccal misoprostol.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsMedical; Abortion, Fetus
CountriesUnited States
CollaboratorsSecretaria de Salud, Mexico

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedOct 22, 2013
Enrollment StartAug 1, 2011
Primary CompletionMay 1, 2012
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 12.7 years ago