Validation and standardization of the measurement of pelvic floor dysfunction with the MAPLE-probe

Completed

• Conditions: pelvic floor; urge urinary incontinence; 10018188

• Registration Number: NL-OMON39307
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 18 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 50

Inclusion Criteria

Patients with pelvic floor dysfunction

Exclusion Criteria

women with neurological diseases

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>To detect significant differences in measurement with the common used probes<br /><br>and the MAPLe.<br /><br><br /><br>To validate the MAPLe.<br /><br><br /><br>To improve complaints of Urgency/Frequency and/or Urge Urinary Incontinence</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Quality of Life</p><br>