The aim of the present study is to determine the efficacy of the placement of an onlay mesh
to prevent incisional hernia after loop ileostomy closure in patients with a prior rectal
resection for cancer
Radiation: Control CT
Other: Clinical Follow Up
Procedure: Reinforcement with Light Polypropylene Mesh
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Full eligibility criteria for NCT02896686
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
patients operated on in hospitals in Catalunya for loop ileostomy closure after a prior rectal resection for rectal cancer.
elective surgery for loop ileostomy closure
ASA (American Society of Anesthesiologists)<4
allergy or intolerance to polypropilene
patients with a prior mesh on the abdominal wall
patients with a life expectancy of <12 months
chronic renal failure in haemodialysis
patients on steroid therapy
All locations for NCT02896686
View full eligibility
Tris trial is registered with FDA with number: NCT02896686. The sponsor of the trial is Hospital Universitari Joan XXIII de Tarragona. and it is looking for 157 volunteers for the current phase.
Official trial title: Multicentric, Prospective, Randomized and Simple Blind Study to Determine the Efficacy of the Placement of an Onlay Mesh for Prevention of Incisional Hernia After Loop Ileostomy Closure in Patients With a Prior Rectal Resection for Cancer
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