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Prevention of Incisional Hernia After Renal Transplantation

NCT04794582 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2024-11-22

No results posted yet for this 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.

Conditions

  • Incisional Hernia
  • Kidney Transplantation
  • Postoperative Complications

Interventions

DEVICE

ProGrip™ Self-Gripping Polyester Mesh

Supra-aponeurotic placement of ProGrip® macroporous polyester mesh in the supra-aponeurotic position

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal

    lead OTHER

Principal Investigators

  • VICTORIA GOMEZ · Fundación para la Investigación Biomédica del Hospital Unive

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-31
Primary Completion
2026-12-31
Completion
2026-12-31
FDA Device
Yes

Countries

  • Spain

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04794582 on ClinicalTrials.gov