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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
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Patients receiving conventional sigmoid end colostomy plus a lightweight mesh Ultrapro® |
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| 2 | Other | Patients receiving conventional sigmoid end colostomy, without mesh |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Mesh (Ultrapro ®) | Device | In the mesh group, the mesh was placed in the sublay position, above the peritoneum and the posterior rectus sheath of the rectus abdominis muscles, with a minimum of 5 cm of mesh around the colostomy |
| Measure | Description | Time Frame |
|---|---|---|
| the reduction in the incidence of Parastomal Hernia after the mesh placement | 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Salvador Navarro-Soto, MD | Corporacio Sanitaria Parc Tauli | Study Chair |
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| Conventional sigmoid end colostomy | Procedure | Patients receiving conventional sigmoid end colostomy, without mesh |
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