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Clinical Trial Summary

To compare the ultrasonographic cervical length with the Bishop score in determining the administration of prostaglandin for preinduction cervical ripening in multiparous women at term.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT01317823
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date December 2008
Completion date April 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 NCT01317862 - A Comparison of Transcervical Foley Catheter and Prostaglandins for Induction of Labor at Term N/A
Completed NCT01506388 - A Novel Protocol for Labour Induction Phase 3
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