Prophylactic Funnel Mesh to Prevent Parastomal Hernia in Permanent End Colostomy After Abdomino-perineal Resection

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04793009

Enrollment

Registered

2021-03-11

Start date

2013-01-01

Completion date

2021-02-28

Last updated

2021-03-11

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

Conditions

Colostomy Stoma, Hernia

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.

Interventions

DEVICEfunnel-shaped, intraperitoneal mesh placement

Implantation of a prophylactic, 3D funnel-shaped, intraperitoneal, non-absorbable and synthetic mesh (Dyna Mesh IPST 2x15x15 cm™ and 3x16x16 cm™, FEG Textiltechnik, Aachen, Germany,)

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* elecitve abdominoperineal resection

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame	Description
Occurrence of parastomal hernia	initial operation until an avarage of 3 years	clinical or radiological diagnosed parastomal hernia

Secondary

Measure	Time frame	Description
Reoperations due to parastomal hernia	initial operation until an avarage of 3 years	Reoperation due to problems caused by parastomal hernia
Mesh-associated complications	initial operation until an avarage of 3 years	any complications due to the mesh

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026