Cervical Ripening Interventions

Status Terminated

Clinical Trial Summary

We wish to determine whether patients undergoing cervical ripening with an infusion of saline will have a lower c-section rate than patients who undergo cervical ripening with misoprostol.

Clinical Trial Description

The primary hypothesis is that patients undergoing cervical ripening with EASI (extra-amniotic saline infusion) catheter have a lower proportion of women who undergo cesarean section for fetal intolerance of labor as compared to misoprostol. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Induction of Labor

Clinical Trial Details

NCT number	NCT00383942
Study type	Interventional
Source	Loyola University
Contact
Status	Terminated
Phase	Phase 3
Start date	July 2006
Completion date	June 2008

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT01127581` - Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery	Phase 3
Completed	`NCT01139801` - Cervical Ripening for Induction of Labor: Misoprostol Versus Oxytocin in Conjunction With Foley Balloon	N/A
Active, not recruiting	`NCT06324279` - Cervical Sliding Sign to Predict Outcome of Induction of Labor
Recruiting	`NCT05864326` - Heated Saline in Cervical Balloon for Labor Induction, a RCT	N/A
Active, not recruiting	`NCT06056141` - Induction of Labour at Term With Low Dose Oral Misoprostol Versus a Foley Catheter	Phase 4
Completed	`NCT04529837` - Ultrasound Assessment of DILAPAN-S
Completed	`NCT02477085` - Methods of Labor Induction and Perinatal Outcomes
Completed	`NCT02098421` - Foley Labor Induction Trial at Term and in PROM	Phase 1
Completed	`NCT03138252` - Study of the Effectiveness of Cervical Ripening Balloon With and Without Oxytocin	Phase 3
Recruiting	`NCT01720394` - Efficacy of Induction of Labor on Term Using a Double Balloon Catheter Compared to Dinoprostone Vaginal-insert	Phase 4
Completed	`NCT00451308` - Induction of Labor With a Foley Balloon Catheter: Inflation With 30ml Compared to 60ml	Phase 4
Not yet recruiting	`NCT05511727` - Use of Single Versus Double Foley's Catheter in Pre-induction Cervical Ripening	N/A
Recruiting	`NCT02762942` - Comparison of Vaginal Misoprostol Plus Supracervical Balloon Versus Vaginal Misoprostol Alone for Induction of Labor	Phase 4
Completed	`NCT01283022` - Pharmacokinetic (PK) Study of the 200 Microgram (mcg) Misoprostol Vaginal Insert (MVI 200) in Women at Term Gestation (The MVI-PK Study)	Phase 2
Recruiting	`NCT00684606` - Transcervical Foley Catheter With or Without Oxytocin for Induction of Labor	N/A
Recruiting	`NCT05759364` - The Effect of IV PAPAVERINE 80 mg Prior to Catheter Balloon Insertion on Bishop Score and Pain	N/A
Recruiting	`NCT03854383` - Using Isosorbide Mononitrate in Reducing Time in Induction of Labor in Post Date Women	Phase 2
Completed	`NCT01428037` - Safety and Efficacy Study of Vaginal Misoprostol for Cervical Ripening and Induction of Labor	Phase 3
Terminated	`NCT03752073` - Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix	N/A
Recruiting	`NCT03045939` - Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours	N/A