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Clinical Trial Summary

The purpose of this clinical trial is to investigate the efficacy of early amniotomy on reducing both the duration of labor and the frequency of dystocia in nulliparous women undergoing an induction of labor. This research project is a prospective, parallel clinical trial, in which subjects are randomized into one of two treatment groups: those who undergo early amniotomy and those who do not undergo early artificial rupture of the amniotic membranes.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT00133016
Study type Interventional
Source University of Pennsylvania
Contact
Status Withdrawn
Phase N/A
Start date August 2006
Completion date August 2006

See also
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Completed NCT04731896 - Early Versus Late Amniotomy During Labor Induction in Women With Bishop's Score of ≥ 6 N/A
Terminated NCT02373800 - Elastography for Evaluating Cervical Maturity in Preparation for Labor Induction at 37 to 42 Weeks of Gestation