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Clinical Trials/NCT04793009
NCT04793009
Completed
Not Applicable

Prophylactic Funnel Mesh to Prevent Parastomal Hernia in Permanent End Colostomy: A Retrospective Cohort Study

Walter Brunner0 sites76 target enrollmentJanuary 1, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hernia
Sponsor
Walter Brunner
Enrollment
76
Primary Endpoint
Occurrence of parastomal hernia
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This retrospective study asses if a prophylactic, funnel-shaped, intraperitoneal mesh prevents parastomal hernia in patients undergoing abdominoperineal rectum resection with permanent end colostomy.

Registry
clinicaltrials.gov
Start Date
January 1, 2013
End Date
February 28, 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Walter Brunner
Responsible Party
Sponsor Investigator
Principal Investigator

Walter Brunner

Leitender Arzt kolorektale Chirurgie

Cantonal Hospital of St. Gallen

Eligibility Criteria

Inclusion Criteria

  • elecitve abdominoperineal resection

Exclusion Criteria

  • rejection of a retrospective data Analysis
  • age under 18 years
  • meshes other than the funnel-shaped mesh

Outcomes

Primary Outcomes

Occurrence of parastomal hernia

Time Frame: initial operation until an avarage of 3 years

clinical or radiological diagnosed parastomal hernia

Secondary Outcomes

  • Reoperations due to parastomal hernia(initial operation until an avarage of 3 years)
  • Mesh-associated complications(initial operation until an avarage of 3 years)

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