drugset / Trial / NCT02633761

Mifepristone-misoprostol vs. Misoprostol Alone for Second Trimester Fetal Death

NCT02633761

Phase 3 Terminated 200 enrolled Gynuity Health Projects
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary aim of this trial is to compare the efficacy of mifepristone-misoprostol versus misoprostol alone for treatment of intrauterine fetal demise between 14 and 28 weeks LMP.

Timeline

Start
2015-04-01
Primary completion
2018-12-30
Completion
2018-12-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Mifepristone Small molecule 200 mg
Comparator Misoprostol Other / unclassified 200 ug Other