drugset / Trial / NCT01231126

Evaluation the Blood Loss in Pregnancies With Misoprostol-induced Labour

NCT01231126

Phase 4 Completed 161 enrolled Maternidade Escola Assis Chateaubriand
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the blood loss in induced vaginal delivery by misoprostol and caesarians section with induction attempt.

Timeline

Start
2008-02
Primary completion
2009-01
Completion
2009-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 25 ug Other

Indications