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Clinical Trial Summary

Demonstrate that with concomitant and synchronous use of supracervical balloon and vaginal misoprostol for induction of labour, vaginal delivery is achieved in less time compared with vaginal misoprostol alone.


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 NCT02762942
Study type Interventional
Source Consorci Sanitari de Terrassa
Contact Àngels Vives Argilagós, MD
Phone +34 937310007
Email MAVives@cst.cat
Status Recruiting
Phase Phase 4
Start date May 2016
Completion date September 2017

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