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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON44885

Enrollment

Registered

2015-02-23

Start date

2015-02-23

Completion date

Unknown

Last updated

2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

mesh complications

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
Subjective improvement at the study visit, measured by PGI-I.	—

Secondary

Measure	Time frame
- Disease specific quality of life at study visit. - Re- interventions after the mesh revision - Anatomical cure of prolapse, measured with POPQ	—

Countries

Netherlands

Outcome results