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Prevention of Incisional Hernia After Renal Transplantation

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Re-verified, no change to tracked fieldsv6
  2. Interventions: ProGrip® Polypropylene Self-Gripping Mesh (Device) to ProGrip™ Self-Gripping Polyester Mesh (Device)
    • Study description shortened, about 5 words
    v5
  3. Re-verified, no change to tracked fieldsv4
  4. Trial status: Not Yet Recruiting to Recruitingv3 Show 5 more changesShow less
    • Primary and study completion dates: Apr 2025 to Dec 2026
    • Start date changed from estimate of Sep 6, 2021 to Aug 31, 2022
    • Primary endpoint revised
    • Secondary endpoints: 3 to 1
    • Site details revised
  5. Start date: Apr 2021 to Sep 6, 2021v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT04794582
Lead Sponsor Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
Collaborators: Medtronic
Conditions
(from sponsor)		 Incisional Hernia, Kidney Transplantation, Postoperative Complications
Related terms Incisional Hernia, Postoperative Complications
Enrollment 160 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov