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RandomizEd ClinicAL triaL on the Efficacy and saFety of Incremental Hemodialysis (REAL-LIFE)

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Enrollment target: 116 to 190v3 Show 7 more changesShow less
    • Primary and study completion dates: Nov 30, 2024 to Dec 31, 2026
    • Primary endpoint revised
    • Eligibility criteria expanded, about 32 words
    • Secondary endpoints: details revised at 4 of 10 entries
    • Study description expanded, about 11 words
    • Collaborators expanded, about 9 words
    • Publications: 5 to 6
  2. Notable Lead sponsor: Carlo Basile, M.D. to Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bariv2 Show 10 more changesShow less
    • Trial status: Not Yet Recruiting to Recruiting
    • Primary completion date: Dec 2023 to Nov 30, 2024
    • Start date changed from estimate of Sep 2020 to May 10, 2021
    • Primary endpoint revised
    • Study completion date: Dec 2024 to Nov 30, 2024
    • Eligibility criteria shortened, about 21 words
    • Secondary endpoints: 9 to 10
    • Study description expanded, about 41 words
    • Study title expanded, about 6 words
    • Collaborators shortened, about 3 words
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Background: The thrice-weekly hemodialysis (HD) regimen is widely accepted as a standard prescription. The concept of incremental dialysis has been established as a possible alternative for patients with preserved diuresis and end-stage renal failure in need of HD. The main problems related to prescription of incremental HD are an arbitrary use of infrequent regimens and the lack of clear standards for incorporating residual kidney function (RKF) in the assessment of HD dose. Several models have been proposed for prescription of incremental dialysis. The latest, the variable target model (VTM), gives more clinical weight to the RKF and allows less frequent HD treatments at lower RKF. Despite increasing evidence derived from observational studies to support the use of incremental HD, RCTs are lacking and, therefore, urgently needed. Methods/Design: The Department of Nephrology, Dialysis and Transplantation of the Azienda Ospedaliero Universitaria Consorziale Policlinico, Bari, Italy and the EUDIAL Working Group of the European Renal Association - European Dialysis Transplant Association (ERA-EDTA) are starting a randomized clinical trial (RCT) in incident HD patients, whose name is "REAL LIFE", by using the acronym of its whole definition: RandomizEd clinicAL triaL on the effIcacy and saFety of incremental haEmodialysis. REAL LIFE is a pragmatic, prospective, multicentre, open label RCT, investigator-initiated, comparing the intervention arm (incremental HD) with the control arm (standard 3HD/wk). The trial, originally conceived by experts at the Division of Nephrology of the Miulli General Hospital, Acquaviva delle Fonti, Italy, consists in starting the HD treatment adopting the new incremental approach guided by the VTM. The primary outcome is the survival of kidney function, with the event defined as urinary output (UO) ≤ 200 mL/day, confirmed by a further collection after 2 weeks to exclude temporary illness. Discussion: REAL LIFE will enable the investigators to know with the highest level of scientific evidence the safety and efficacy of an incremental approach to the start of HD treatment.
Trial Details
NCT Number NCT04360694
Lead Sponsor Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Collaborators: European Renal Association - European Dialysis and Transplant Association
Conditions
(from sponsor)
End Stage Renal Disease on Dialysis
Enrollment 190 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov