PREGNANT Short Cervix Trial

Status Completed

Clinical Trial Summary

The purpose of this research study is to evaluate the usefulness of progesterone vaginal gel in decreasing the preterm birth rate in a population of pregnant women with short cervical length and at high risk for preterm birth.

Clinical Trial Description

A Short uterine cervical length in the mid-trimester is the most powerful predictor of preterm birth. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00615550
Study type	Interventional
Source	Juniper Pharmaceuticals, Inc.
Contact
Status	Completed
Phase	Phase 3
Start date	March 2008
Completion date	November 2010

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