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Trials / Completed

CompletedNCT00901758

Intravenous (IV) Nitroglycerin for Versions in Multiparous Women

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
44 (actual)
Sponsor
University of Calgary · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

Breech presentations (where a baby presents with feet or bottom down) have an increased risk of perinatal and neonatal complications, and are usually delivered by cesarean section. As an alternative, so that the baby can be delivered vaginally, an attempt can be made to turn the baby so that it is head down: this manoeuvre is called an external cephalic version (ECV). Drugs that relax the uterus (tocolytic agents) are sometimes used to help improve ECV success rates. Nitroglycerin is a tocolytic agent, but intravenous nitroglycerin has not been tested as an agent to help ECV. There is some suggestion that nitroglycerin may be more helpful in women who have not previously been pregnant (nulliparous women) than in women who have been pregnant more than once (multiparous women), and so we have planned two trials. This study is designed to answer the following questions for multiparous women: Will administration of IV nitroglycerin for uterine relaxation improve ECV success rates? Will an increase in ECV success result in a decreased cesarean section rate?

Conditions

Interventions

TypeNameDescription
DRUGIV NitroglycerinIV injection, initial does of 1mL, with further doses of 1-3mL, up to a recommended maximum of 10mL.
DRUGNormal salineIV injection, initial does of 1mL, with further doses of 1-3mL, up to a recommended maximum of 10mL

Timeline

Start date
2003-03-01
Primary completion
2006-10-01
Completion
2008-02-01
First posted
2009-05-14
Last updated
2013-08-28

Locations

3 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00901758. Inclusion in this directory is not an endorsement.

Intravenous (IV) Nitroglycerin for Versions in Multiparous Women (NCT00901758) · Clinical Trials Directory