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

Walter Brunner

Status: Completed

Conditions: Colostomy Stoma; Hernia

Treatments: Device: funnel-shaped, intraperitoneal mesh placement

Study type: Observational

Funder types: Other

Identifiers

NCT04793009

2021-00120 (Other Identifier)

CHIR2021WB

Details and patient eligibility

About

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

Enrollment: 76 patients

Sex: All

Ages: 18+ years old

Volunteers: No 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

Trial design

76 participants in 2 patient groups

mesh group

Description:

patients undergoing abdominoperineal resection with end colostomy and implantation of a prophylactic, funnel-shaped, intraperitoneal mesh

Treatment:

Device: funnel-shaped, intraperitoneal mesh placement

no-mesh group

Description:

patients undergoing abdominoperineal resection with end colostomy without implantation of a prophylactic, funnel-shaped, intraperitoneal mesh