Trials / Completed
CompletedNCT04793009
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
- Phase
- —
- Study type
- Observational
- Enrollment
- 76 (actual)
- Sponsor
- Walter Brunner · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | funnel-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,) |
Timeline
- Start date
- 2013-01-01
- Primary completion
- 2018-12-31
- Completion
- 2021-02-28
- First posted
- 2021-03-11
- Last updated
- 2021-03-11
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04793009. Inclusion in this directory is not an endorsement.