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Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix — CORC  

Induction of Labor Clinical Trial

Official title:
Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix

Clinical Trial Summary

This is a randomized prospective trial of two mechanical methods of pre-induction cervical ripening agents.

Clinical Trial Description

Term, low risk patients requesting elective induction of labor who desire pre-induction cervical ripening at home will be randomized to receive an outpatient trans-cervical ripening balloon (17 F non-latex Foley catheter) or hygroscopic cervical dilator (Dilapan-S). Patients present to the hospital for their scheduled induction of labor approximately 12 hours later. We hypothesize that the trans-cervical balloon and hygroscopic dilators will show equivalent efficacy in cervical ripening, but that pain scores and patient satisfaction will be better with the hygroscopic dilators. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03752073
Study type Interventional
Source Ochsner Health System
Contact
Status Terminated
Phase N/A
Start date March 1, 2019
Completion date January 1, 2023
View Details
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