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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 nulliparas 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 NCT01317706
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date November 2008
Completion date August 2010

See also
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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 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