Efficacy of revision of mesh surgery in patients with complications after treatment with vaginal synthetic mesh.

Completed

• Conditions: mesh complications; 10029903

• Registration Number: NL-OMON44885
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 53

Inclusion Criteria

All patients that have been operated between 2009 and 2014 in the Academic Medical Center or Bergmanclinics Vrouwenzorg, because of complications due to vaginal mesh surgery (exposure or pain).

Exclusion Criteria

Patients with mesh compliations that haven't been operated because of this complication.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Subjective improvement at the study visit, measured by PGI-I.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- Disease specific quality of life at study visit.<br /><br>- Re- interventions after the *mesh revision*<br /><br>- Anatomical cure of prolapse, measured with POPQ</p><br>