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Cervical Pessary to Prevent Preterm Birth in Singleton Pregnancies With a Sonographically Measured Short Cervix

Premature Birth Clinical Trial

Official title:
Cervical Pessary to Prevent Preterm Birth in Singleton Pregnancies With a Sonographically Measured Short Cervix: an Open-label Randomized Controlled Trial

Clinical Trial Summary

The purpose of this study is to learn if the Arabin pessary can reduce preterm birth less than 37 weeks 0 days in singleton pregnancies that have a short cervix.

Clinical Trial Description

This is an open label randomized controlled study. The pessary will be offered to those patients who have a transvaginal cervical length less than 25 mm before 23 weeks 0 days. The control group will receive the current standard of care which includes surveillance of cervical length, vaginal progesterone, and emergency cerclage. The primary outcome of the study is preterm delivery less than 37 weeks 0 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02357394
Study type Interventional
Source University of Kansas Medical Center
Contact
Status Terminated
Phase N/A
Start date May 2015
Completion date April 1, 2019
View Details
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