drugset / Trial / NCT00466128

Indomethacin Versus Placebo in Women With Preterm Premature Rupture of Membranes (PPROM)

NCT00466128

Phase 2 Unknown 116 enrolled Thomas Jefferson University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine if the short term use of indomethacin will reduce the number of women delivering within 48 hours when given to women with preterm premature rupture of membranes (PPROM) between 24- 32 weeks of gestation. We hypothesize that indomethacin's anti-inflammatory and tocolytic action will reduce the number of women delivering within 48 hours when given to women with PPROM between 24-32 weeks of gestation.

Timeline

Start
2007-04
Primary completion
2015-04
Completion
2016-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Indomethacin Small molecule 25 mg Oral