Use of a Mesh to Prevent Parastomal Hernia

Status Completed

Clinical Trial Summary

Randomized, controlled, prospective study of 54 patients receiving surgery for cancer of the lower third of the rectum with a permanent end colostomy. The aim of the study was to reduce parastomal hernia (PH) occurrence by implanting a lightweight mesh in the sublay position. Patients were followed up a) clinically and b) radiologically by means of abdominal CT. In the clinical follow-up, hernias were observed in four out of 27 patients (14.8%) in the study group and in eleven out of 27 (40.7%) in the control group (p=0.03). The implantation of the mesh reduces the appearance of PH, is well tolerated, and does not increase morbidity

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00691860
Study type	Interventional
Source	Corporacion Parc Tauli
Contact
Status	Completed
Phase	N/A
Start date	April 2006
Completion date	February 2008

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See also
Status	Clinical Trial	Phase
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Completed	`NCT01380860` - Primary Prevention of Peristomial Hernias Via Parietal Prostheses	N/A
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Completed	`NCT02368873` - the Use of a IPOM Mesh for Prevention of Parastomal Hernia	N/A
Completed	`NCT02233465` - Treating Parastomal Hernia With a Mesh	Phase 1/Phase 2
Completed	`NCT00917995` - Trial Concerning the Frequency of Parastomal Hernia With or Without a Mesh	Phase 2/Phase 3
Completed	`NCT01484743` - Risk Factors for Morbidity After Parastomal Hernia Repair
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