BRAVO study: Bladderscan validation study for asymptomatic postpartum urinary retentio

• Conditions: 10010273; Asymptomatic postpartum urinary retention; inadequate voiding after delivery

• Registration Number: NL-OMON37324
• Lead Sponsor: Catharina-ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 1000

Inclusion Criteria

Women >= 18 years
after vaginal delivery

Exclusion Criteria

women < 18 years
after cesarean section

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Reliability of the Bladderscan</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>1. Prevalence of asymptomatic postpartum urinary retention<br /><br>2. Risk profile for asymptomatic postpartum urinary retention</p><br>