Actively Recruiting
RandomizEd ClinicAL triaL on the Efficacy and saFety of Incremental Hemodialysis (REAL-LIFE)
Led by Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari · Updated on 2024-06-12
190
Participants Needed
1
Research Sites
294 weeks
Total Duration
On this page
Sponsors
A
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Lead Sponsor
E
European Renal Association - European Dialysis and Transplant Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
RandomizEd ClinicAL triaL on the Efficacy and saFety of Incremental Hemodialysis (REAL-LIFE)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged > 18 years
- Patients starting maintenance hemodialysis for advanced chronic kidney disease stage 5D
- Patients starting hemodialysis now or within the past 2 weeks
- Estimated glomerular filtration rate (eGFR) ≤ 10 mL/min/1.73 m2 as calculated by CKD-EPI formula
You will not qualify if you...
- Age under 18 years
- Acute kidney injury or acute on chronic kidney injury
- eGFR greater than 10 mL/min/1.73 m2
- Urine output less than 600 mL per day
- Previous treatment with other kidney replacement therapies such as peritoneal dialysis or kidney transplant
- Unable or unwilling to give informed consent
- Unable to follow trial procedures including urine output collection
- Expected survival less than 6 months or planned change of treatment center or modality within 6 months
- Listed for living kidney transplant
- Active cancer or refractory congestive heart failure (type IV NYHA, ejection fraction ≤ 30%) requiring high ultrafiltration volume per session
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Trial Site Locations
Total: 1 location
1
Azienda Ospedaliero Universitaria Consorziale Policlinico
Bari, Italy, 70124
Actively Recruiting
Research Team
L
Loreto Gesualdo, MD
CONTACT
D
Domenico Roselli, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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