Sexual function following the MiniArc procedure

Completed

• Conditions: seksuele functie; sexual function

• Registration Number: NL-OMON33286
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

- female patients who will undergo the MiniArc procedure for stress urinary incontinence
- >18 years old
- in a relationship with a partner

Exclusion Criteria

- medical histery of vaginal surgery
- <18 years old
- patients who do not speak Dutch

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>A. To determine the effect of a MiniArc procedure on female sexual function in<br /><br>relation to the surgical procedure and it's treatment result.<br /><br>B. Also to evaluate the determinants/causal factors of this effect.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Parameters/outcome:<br /><br>• anwsers to the general questions<br /><br>• the (subjective) treatment result<br /><br>• total score FSFI preoperatively compared to postoperatively<br /><br>• subscores of the GRISS preoperatively compared to postoperatively<br /><br>• subscores of the GRISS of the partner preoperatively compared to<br /><br>postoperatively<br /><br>• anwsers to the questions about sexuality by the partners preoperatively<br /><br>compared to postoperatively</p><br>