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Clinical Trial Summary

The purpose of this study is to assess the effectiveness and safety of transcervical foley catheter as compared to prostaglandins for preinduction cervical ripening and labor induction in term nulliparous women with unfavorable cervix.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01317862
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date January 2011
Completion date September 2012

See also
  Status Clinical Trial Phase
Completed NCT02618096 - Concurrent Oxytocin With Membrane Sweeping Versus Dinoprostone Pessary in Labor Induction of Multiparous Women at Term N/A
Completed NCT01317706 - Comparison Between Ultrasonographic Cervical Length and Bishop Score in Preinduction Cervical Assessment N/A
Completed NCT01596296 - Foley Catheter Versus Dinoprostone Vaginal Insert for Induction of Labor in Parous Women at Term: A Randomized Trial N/A
Completed NCT02485821 - Vaginal Estradiol Pretreatment in Labour Induction With Misoprostol Phase 2/Phase 3
Completed NCT02314260 - Modifying Cervical Bishop Scoring System N/A
Completed NCT01506388 - A Novel Protocol for Labour Induction Phase 3
Completed NCT01317823 - Bishop Score and Transvaginal Ultrasound for Preinduction Cervical Assessment in Multiparas N/A
Completed NCT02524002 - Enhanced vs. Routine Clear Liquid Intake in Labor N/A
Completed NCT02416583 - Concurrent Oxytocin With Membrane Sweeping Versus Dinoprostone Pessary in Labor Induction of Nulliparas at Term N/A