DIALysis with EXpanded Solute Removal

Not Applicable

Not yet recruiting

• Conditions: Chronic Kidney Disease Requiring Hemodialysis; End-Stage Kidney Disease (ESKD)

• Registration Number: NCT06660277
• Lead Sponsor: Western University, Canada

Brief Summary

The goal of this clinical trial is to evaluate the health effects of expanded hemodialysis in patients receiving hemodialysis. The main question it aims to answer is:

1) Does expanded hemodialysis reduce the risk of death from any cause?

Researchers will compare expanded hemodialysis to conventional hemodialysis (the treatment currently used for the majority of patients receiving hemodialysis) to see if expanded hemodialysis works to improve patient outcomes.

Participants will continue to receive their regularly scheduled hemodialysis treatments using either a super high-flux/expanded dialysis filter or a high-flux/conventional dialysis filter. All other aspects of treatments remain the same. No additional tests or visits are required. Data will be obtained using administrative healthcare databases.

Detailed Description

Background:

Expanded hemodialysis refers to hemodialysis treatment using a newer generation of hemodialysis filters or "dialyzers" that remove large middle molecules to a greater extent than conventional "high-flux" dialyzers. This is expected to improve major health outcomes. However, despite a decade of availability and promising surrogate data from small trials and patient outcomes data from large observational studies, dialyzers capable of providing expanded hemodialysis have failed to achieve significant adoption conventional high-flux dialyzers in the absence of more definitive evidence. A large, rigorous randomized controlled trial is necessary to establish the clinical effectiveness of expanded hemodialysis compared to conventional hemodialysis with high-flux dialyzers.

Study Design:

Parallel, block randomized, controlled, open label, superiority trial comparing the clinical effects of expanded hemodialysis using Nipro Elisio HX dialyzers to conventional hemodialysis using high-flux dialyzers. The allocation ratio will vary between 1:3 or 1:1 ratio depending on their dialysis unit.

Setting:

Community and academic hemodialysis facilities.

Study Size:

4800 participants (1200 in expanded hemodialysis arm and 3600 in conventional high-flux hemodialysis arm) followed for a mean of 2.9 years.

Trial Duration:

Duration of participant accrual - 2 years from date of first participant recruited.

Total duration - 5 years from date of first participant recruited. Trial results anticipated to be announced in 2030.

Study Power:

90% power to detect 15% relative reduction in the hazard of death (hazard ratio 0.85).

Study Timeline

• Status Verified: 2024-09
• Study First Submitted: 2024-10-23
• Study First Submitted QC: 2024-10-23
• Study First Posted: 2024-10-28
• Last Update Submitted: 2024-11-21
• Last Update Posted: 2024-11-26
• Study Start: 2025-01
• Primary Completion: 2030-01
• Study Completion: 2030-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 4800

Inclusion Criteria

Inclusion requires that all the following are present:

1. Age 60 years or older, or age 45 to 59 years and using medication to treat diabetes;
2. Receiving any form of dialysis regularly for the previous 3 months; and
3. Currently receiving hemodialysis in-centre (main or satellite unit) 3 or more times per week.

Exclusion Criteria

Patients are ineligible if they meet any of the following criteria:

1. Not appropriate for this study in the opinion of the treating nephrologist or dialysis nurse practitioner due to any of:

   1. Known or anticipated intolerance to the Nipro Elisio HX dialyzer
   2. Planned to receive hemodiafiltration
   3. Planned to receive nocturnal hemodialysis
   4. Anticipated to discontinue in-centre hemodialysis in the next 3 months for any reason (examples: palliation, transplantation, home dialysis, recovery of kidney function, death, others)
   5. Anticipated severe non-adherence to the frequency or duration of prescribed dialysis treatment

2. Previously enrolled in this trial

3. Declined participation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Primary Outcome of All-Cause Mortality	From enrollment to event (death) or end of treatment (average 2.9 years), whichever occurs first	All-cause mortality will be ascertained using Canada Vitals Statistics Dataset from Statistics Canada. All-cause mortality is recorded with over 99% accuracy in our data sources.

Secondary Outcome Measures

Name	Time	Method
Key Secondary Outcome of Cardiovascular and Infection-Related Hospitalizations	From enrollment to end of treatment (average 2.9 years)	Cardiovascular and infection-related hospitalizations will be ascertained using primary discharge ICD-10 diagnosis codes in the Canadian Institute for Health Information Discharge Abstract Database
Cardiovascular-Related Hospitalizations	From enrollment to end of treatment (average 2.9 years)	Each component of the secondary outcome (cardiovascular-related and infection-related hospitalizations) will be examined separately.
Infection-Related Hospitalizations	From enrollment to end of treatment (average 2.9 years)	Each component of the secondary outcome (cardiovascular-related and infection-related hospitalizations) will be examined separately.

Trial Locations

Locations (1)

London Health Sciences Centre; 🇨🇦 London, Ontario, Canada