Polypropylene Mesh in Prolapse Surgery

Polypropylene Mesh in Prolapse Surgery; Long-term Outcome and Complications.

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02383199

Enrollment

161

Registered

2015-03-09

Start date

2013-09-30

Completion date

2014-11-30

Last updated

2015-03-27

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

Conditions

Pelvic Organ Prolapse

Brief summary

The purpose of this study was to report the long-term objective and subjective outcome after prolapse surgery with polypropylene mesh. The complications and the effect of the learning curve of the surgeons to the outcome is also reported.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Healthy volunteers

Inclusion criteria

195 first patients with pelvic organ prolapse operated on using polypropylene mesh

Design outcomes

Primary

Measure	Time frame	Description
Subjective outcome with validated questionnaires	7 years	Validated questionnaires

Secondary

Measure	Time frame	Description
Objective outcome: anatomic outcome with Pelvic Organ Prolapse Quantification (POP-Q) system	7 years	—
Number of patients with adverse events and reoperations.	7 years	POP-Q

Outcome results