drugset / Trial / NCT00892229

Buccal Versus Vaginal Misoprostol in Surgical Termination of the First Trimester Missed Abortion in Erbil

NCT00892229

Phase 2 Completed 100 enrolled Hawler Medical University NEGATIVE · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the effectiveness of buccal misoprostol and comparing this with vaginal route of the same drug.

Timeline

Start
2007-03
Primary completion
2008-01
Completion
2008-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Misoprostol Other / unclassified 400 ug Other