The use of foley catheter results in less interventions as compared to the use of propess

Phase 3

Completed

• Conditions: ripening/priming; 10026906

• Registration Number: NL-OMON32840
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 194

Inclusion Criteria

single pregnancy at term who has a bishop score lower than 6

Exclusion Criteria

broken membranes/who have had a sectio/bad foetal condition

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>percentage of caesarean sectio</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- bishop 6 or higher after treatment<br /><br>- neonatale outcome<br /><br>- fever<br /><br>- the amount of syntocinon<br /><br>- total gifts of propess<br /><br>- time to delivery<br /><br>- total costs<br /><br>- anesthesia</p><br>