Safety & Efficacy of Dinoprostone (Propess) in the Women With Premature

See also
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Completed	`NCT04529837` - Ultrasound Assessment of DILAPAN-S
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Completed	`NCT02098421` - Foley Labor Induction Trial at Term and in PROM	Phase 1
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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

NCT number	NCT01916291
Study type	Interventional
Source	Seoul National University Hospital
Contact
Status	Completed
Phase	Phase 2
Start date	August 25, 2013
Completion date	April 4, 2019

Safety and Efficacy of Dinoprostone (Propess) in the Women With Premature Rupture of Membrane or Gestational Age <38

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms