Prophylactic Mesh in Cytoreductive Surgery

Status Not yet recruiting

Clinical Trial Summary

Evaluate the effectiveness of mesh reinforcement in high-risk patients to prevent incisional hernia.

Clinical Trial Description

Based on the hypothesis that oncological cytoreductive surgery plus hyperthermic intraperitoneal chemotherapy (HIPEC) is associated with an increased risk of developing Incisional Hernia in the postoperative period, with an expected incidence of 50% at 24 months, we designed a prospective, multicenter and randomized clinical study to demonstrate the utility of the meshes in the prevention of Incisional Hernia, hoping to reduce the incidence to 15% at 24 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03953365
Study type	Interventional
Source	Hospital Universitario Fundación Alcorcón
Contact
Status	Not yet recruiting
Phase	N/A
Start date	June 1, 2019
Completion date	December 31, 2023

View Details

See also
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