A Randomized, Control Trial for Preinduction Cervical Ripening

Status Completed

Clinical Trial Summary

The goal of this study is to compare the vaginal delivery rates in women undergoing induction of labor with an unripe cervix between oxytocin induction alone and preinduction cervical ripening with prostaglandin El (misoprostol). Secondary goals are to measure and compare the time intervals to delivery between the two methods.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Labor, Induced

Clinical Trial Details

NCT number	NCT00393731
Study type	Interventional
Source	The University of Texas Health Science Center, Houston
Contact
Status	Completed
Phase	Phase 2
Start date	January 2004
Completion date	August 2007

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT02902653` - Efficacy and Safety of Hourly Titrated Misoprostol Versus Vaginal Dinoprostone and Misoprostol for Cervical Ripening and Labor Induction	Phase 4
Completed	`NCT05100264` - Effect of Acidic Vaginal pH on the Efficacy of Dinoprostone for Labor Induction	N/A
Completed	`NCT01962831` - Randomized Controlled Trial: Induction of Labour of Obese Women With Dinoprostone or Single Balloon Catheter	N/A
Recruiting	`NCT05857059` - Misoprostol for Induction of Labor in Obese Women: Comparison Between 25 and 50 mcg Oral Administration	N/A
Completed	`NCT03665688` - Comparing Outpatient to Inpatient Cervical Ripening Using Dilapan-S®	N/A
Completed	`NCT00992524` - Oral Titrated Misoprostol for Induction of Labour	N/A
Completed	`NCT00259103` - Recombinant Human Relaxin (rhRlx) in Pregnant Women Scheduled for Induction of Labor	Phase 2
Completed	`NCT04755218` - Labor Induction With Oral Versus Vaginal Misoprostol
Completed	`NCT04746248` - Outpatient Labor Induction Using Oral Misoprostol in Norway	N/A
Completed	`NCT05838313` - Should I Have an Elective Induction?	N/A
Completed	`NCT03140488` - Oxytocin Dosage to Decrease Induction Duration	Phase 4
Recruiting	`NCT02486679` - A Trial of Prostaglandin E2 Tablets Versus Foley Catheter for Labor Induction	Phase 4
Terminated	`NCT01641601` - Prehospital Cervical Ripening Before Induction and the Maternal Experience	N/A
Completed	`NCT00465998` - Study of Ultrasound Imaging to Predict Time and Outcome in Pregnancies With Induced Labor	N/A
Completed	`NCT00545194` - Cervical Ripening Before Induction of Labour at Term: a Randomised Comparison of Prostin vs Propess	Phase 3
Completed	`NCT05874024` - Induction of Labour With a Double Balloon Catheter
Completed	`NCT03407625` - Foley Bulb With Oral Misoprostol for Induction of Labor	N/A
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
Completed	`NCT05885087` - 'Extended Balloon Catheter' Labour Induction; a Single Arm Pilot Trial'	N/A