ProGrip™ Self-Gripping Polyester Mesh: Supra-aponeurotic placement of ProGrip® macroporous polyester mesh in the supra-aponeurotic position
Study summary
Randomized clinical trial to determine the efficacy of mesh reinforcement in laparotomy closure in renal transplantation as measured by reduction in the incidence of incisional hernia at 2 years post-transplantation.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Candidate for first kidney transplant
Exclusion Criteria:
* Patient receiving a second or successive renal transplant.
Primary outcome measure(s)
To determine the efficacy of mesh reinforcement in laparotomy closure in renal transplantation measured by radiological diagnosis (CT) — 24 months To determine the efficacy of mesh reinforcement in laparotomy closure in renal transplantation measured by radiological diagnosis (CT) of incisional hernia at 2 years post-transplantation.
Trial sites (1)
Facility
City
Region
Status
Hospital Universitario Ramón y Cajal
Madrid
Spain
Recruiting
More Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal trials in Spain
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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