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Eplerenone in Patients Undergoing REnal Transplant (EPURE TRANSPLANT)

Study acronym: EPURE
StatusActive, Not Recruiting
PhasePhase 3
Started
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Record History

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  1. Minor Re-verified, no change to tracked fieldsv9
  2. Notable Primary completion date changed from estimate of Jul 2020 to Nov 9, 2021v8 Show 4 more changesShow less
    • Trial status: Recruiting to Active, Not Recruiting
    • Study completion date: Jul 2030 to Aug 2031
    • Start date: Oct 2016 to Oct 19, 2016
    • Site details revised at 7 of 7 sites
  3. Minor Site details revised at 1 of 7 sitesv7
  4. Minor Re-verified, no change to tracked fieldsv6
  5. Minor Interventions: Eplerenon (Drug), Placebo (Drug) to Eplerenone (Drug), Placebo (Drug)
    • Eligibility criteria revised
    • Secondary endpoints: 14 to 13
    • Study sites revised (7)
    v5
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  1. Notable Trial status: Not Yet Recruiting to Recruitingv4 Show 6 more changesShow less
    • Start date: May 2016 to Oct 2016
    • Study sites: 6 to 7
    • Primary completion date: Aug 2020 to Jul 2020
    • Study completion date: May 2030 to Jul 2030
    • Eligibility criteria expanded, about 15 words
    • Secondary endpoints: 13 to 14
  2. Notable Primary completion date: Aug 2019 to Aug 2020
    • Start date: Nov 2015 to May 2016
    • Study completion date: May 2029 to May 2030
    v3
  3. Minor Secondary endpoints revised (13)v2
  1. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Assess the impact of eplerenone (initiated within 2 hours prior to patient departure to the operating room and administered for 4 days during the post-operative period) on graft function evaluated by the measurement of glomerular filtration rate at 3 months - variable strongly associated with long-term graft survival.
Trial Details
NCT Number NCT02490904
Lead Sponsor Central Hospital, Nancy, France
Conditions
(from sponsor)
End-stage Renal Disease
Related terms Kidney Failure, Chronic
Enrollment 132 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov