Clinical Trials Directory

Trials / Completed

CompletedNCT00442663

Trial of Foley Catheter With and Without Extra-Amniotic Saline Infusion for Labor Induction

Randomized Trial of Transcervical Foley Catheter With and Without Extra-Amniotic Saline Infusion for Labor Induction

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
170 (planned)
Sponsor
University of Alabama at Birmingham · Academic / Other
Sex
All
Age
15 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare the efficacy of a transcervical Foley catheter with and without extra-amniotic saline infusion (EASI) for priming the cervix for labor.

Detailed description

In the United States, labor inductions have increased from 11% of all pregnancies in 1989 to 21% in 2004. Although the indications for labor induction vary, labor inductions as an obstetrical practice are associated with an increased risk of Cesarean delivery. As such, the rise in labor inductions has been paralleled by a rise in the cesarean rate to an all time high of 30%. The risk of cesarean can be mitigated with the use of cervical ripening agents in the setting of an unfavorable cervix. Both pharmacological ripening agents and mechanical methods are currently available for cervical priming. Methods available for mechanical dilation include, but are not limited to transcervical foley catheter alone and transcervical foley catheter with an extra-amniotic saline infusion or EASI. The potential advantage of EASI to transcervical foley catheter alone is the promotion of endogenous prostaglandin release by membrane stripping and supplying additional mechanical force. It may be disadvantageous by increasing the risk of chorioamnionitis or by diluting the prostaglandins that are released by membrane stripping. There have been two randomized trials comparing foley alone to foley with EASI. Because the results of these two trials are conflicting, we chose to conduct a randomized clinical trial of foley catheter compared to foley catheter with an EASI for labor induction and cervical ripening in women with an unfavorable cervix.

Conditions

Interventions

TypeNameDescription
DEVICETranscervical Foley Catheter
DEVICETranscervical Foley Catheter with an EASI

Timeline

Start date
2003-06-01
Completion
2005-12-01
First posted
2007-03-02
Last updated
2007-04-24

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00442663. Inclusion in this directory is not an endorsement.