drugset / Trial / NCT00677755

Medical Abortion for Emergency Contraception Failure

NCT00677755

Completed 394 enrolled Taizhou Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the efficacy, safety and acceptability of pre-treatment with mifepristone and misoprostol compared to misoprostol alone in the medical termination of pregnancy by mifepristone EC failure.

Timeline

Start
2004-10
Primary completion
2007-09
Completion
2007-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Mifepristone Small molecule 200 mg Oral
Background Misoprostol Other / unclassified 0.8 mg Oral

Indications

No indication recorded.