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Labor Induction clinical trials

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NCT ID: NCT05257187 Withdrawn - Labor Induction Clinical Trials

Foley Catheter Induction

Start date: November 7, 2021
Phase: N/A
Study type: Interventional

The foley catheter (single lumen balloon) is one of the most cost effective, readily available methods for cervical ripening to begin an induction of labor. It is most commonly used in conjunction with oxytocin, a medication given to induce contractions. However, there is no clear timeline for when to remove the foley catheter or how long foley catheters can be safely kept in place. The study team's goal is to conduct a randomized controlled trial (RCT) in nulliparous and multiparous patients to determine the optimal length of time to retain foley catheters (single balloon) for induction of labor to achieve vaginal delivery while shortening the overall length of labor. Based on our power analysis, the study team plans to enroll a total of 356 patients (218 nulliparous patients and 138 multiparous patients) over the course of 18 months. Then the study team will randomize patients to one of the following two groups: foley catheter removal after 6 hours or foley catheter removal after 12 hours. All patients will receive simultaneous pitocin and a foley catheter, and the remainder of the induction course (i.e. rupture of membranes, etc.) will be left to the discretion of the obstetric provider. The primary outcome will be time of foley catheter insertion to delivery. Secondary outcomes will be rates of cesarean delivery and obstetric/neonatal outcomes.

NCT ID: NCT03218735 Withdrawn - Labor Induction Clinical Trials

Early Term Delivery Versus Expectant Management of the Large for Gestational Age Fetus

TEAM LGA
Start date: July 12, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the incidence of composite neonatal morbidity and birthweight >4500 grams among uncomplicated large for gestational age (LGA) fetal growth at delivered 37 weeks versus expectant management.

NCT ID: NCT00771511 Withdrawn - Labor Pain Clinical Trials

Cervical Capsaicin for Labor Induction and Pain Relief

Start date: October 2010
Phase: Phase 4
Study type: Interventional

In the setting of fetal demise it is important to help the mother deliver the fetus expeditiously and with as little physical trauma as possible. This study hypothesizes that application of capsaicin to the uterine cervix will enhance cervical ripening and desensitize pain fibers such that delivery is less painful.