drugset / Trial / NCT00383942

Ripening Interventions: Prostaglandins vs EASI Catheter

NCT00383942

Phase 4 Terminated 80 enrolled Loyola University
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary aim of this randomized clinical trial is to compare the effect of misoprostol vs extra amniotic saline infusion via a catheter (EASI) for cervical ripening on the proportion of patients delivered by cesarean section for fetal intolerance of labor versus vaginal delivery. The primary hypothesis is that patients undergoing cervical ripening with EASI catheter are less likely to undergo cesarean section for fetal intolerance of labor when compared to women who receive misoprostol.

Timeline

Start
2006-08-31
Primary completion
2008-06-18
Completion
2008-06-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Misoprostol Other / unclassified 25 ug Other

Indications

No indication recorded.