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Cervical Incompetence clinical trials

View clinical trials related to Cervical Incompetence.

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NCT ID: NCT03311867 Completed - Clinical trials for Cervical Incompetence

Prolene Versus Ethibond for Cervical Cerclage

PECC
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The purpose of the proposed study is to examine the relationship between cerclage suture material of Ethibond and Prolene and its effect on the vaginal microbiome in a prospective randomized control trial. Ethibond is another commonly used suture material for performing cervical cerclage that shares some characteristics with previously studied suture materials. It is braided like the Mersilene, but thinner like the monofilament Prolene. The investigators will study whether Ethibond causes the vaginal microbiome to be adversely affected like Mersilene or whether there is a healthy microbiome like Prolene. This study will allow the investigators to determine whether it is advisable to continue to use Ethibond for cervical cerclage in clinical practice, or whether obstetricians should avoid its use as now done with Mersilene.

NCT ID: NCT03305575 Completed - Clinical trials for Cervical Incompetence

Intrathecal Chloroprocaine vs. Bupivacaine for Cervical Cerclage

Start date: October 13, 2017
Phase: Phase 4
Study type: Interventional

This study aims to compare the effect of chloroprocaine vs. bupivacaine on duration of motor block and duration until meeting discharge criteria in patients undergoing cervical cerclage. The hypothesis is that chloroprocaine will result in faster resolution of motor block.