drugset / Trial / NCT01206998

Vaginal Progesterone as a Treatment for Women Active Preterm Labor

NCT01206998

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to compare how well vaginal progesterone works delaying the time to delivery in women with preterm labor compared to placebo. The study will also compare the effect of vaginal progesterone on neonatal outcomes, rate of spontaneous preterm delivery, cervical length and biomarkers of preterm delivery in women diagnosed with and treated with medication to stop preterm labor.

Timeline

Start
2010-07
Primary completion
2010-08
Completion
2010-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Progesterone Other / unclassified 90 mg Other

Indications

No indication recorded.