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CompletedNCT04381234SAFEUpdated May 21, 2020

Strategies for Asymmetrical Triacetate Dialyzer Heparin-Free Effective Hemodialysis

A Phase 2 interventional study of dialyzer and hemodialysis with citrate-containing dialysate in Hemodialysis Complication, sponsored by Universitaire Ziekenhuizen KU Leuven. Completed at 1 site in Belgium. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-05-21.

Sponsored by Universitaire Ziekenhuizen KU Leuven · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 3 months after the study started (first participant enrolled Jan 2018, registered May 2020).
Phase
Phase 2
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Not all dialysis patients tolerate heparin anticoagulation. Heparin should be avoided in patients at high risk of bleeding. Strategies include saline infusion, citrate-containing dialysate, regional citrate anticoagulation and heparin-coated membranes. We recently studied the combination of a heparin-coated membrane and citrate-containing dialysate, with a success rate of 94% . Although this combination resulted in low rates of clotting, heparin-coated membranes are not ubiquitously available. The quest for easy to perform, safe and affordable heparin-free dialysis is on. Asymmetric cellulose triacetate (ATA) dialyzers have a low degree of platelet contact activation and might be an alternative to heparin-coated dialyzers.

This is a phase II pilot study in maintenance dialysis patients. Study design is a two-arm open-label cross-over study. In Arm 1, patients were dialyzed using a 1.9 m2 ATA membrane (Solacea™-19H, Nipro Corp., Japan) in combination with citrate (1 mM) containing dialysate. In Arm 2, patients were dialyzed with the same 1.9 m2 ATA membrane, in combination with high volume predilution hemodiafiltration. The primary endpoint was the success rate to complete 4 hours of hemodialysis without preterm clotting.

Read the detailed description

Anticoagulation is one of the supporting pillars of chronic hemodialysis (HD). The optimal anticoagulant regimen provides full anticoagulation of the extracorporeal circuit with minimal systemic effects and comes at an affordable cost. Unfractionated heparin (UFH) has been the standard of care for many years. In several countries, UFH has gradually been replaced by low molecular weight heparins (LMWH). LMWH are easy to use as they can be administered as a bolus injection and reduce membrane fibrin and platelet deposition. Both UFH and LMWH provide adequate anticoagulation of the extracorporeal circuit, at the price of systemic anticoagulation. Apart from bleeding, the administration of unfractionated heparins has also been associated with dyslipidemia, hypoaldosteronism and hyperkalemia, thrombopenia, osteoporosis, pruritus, and hypersensitivity reactions.

Several alternative anticoagulation regimens have been proposed including saline infusion, heparin coating of the dialyzer membrane as well as regional citrate anticoagulation. Regional citrate anticoagulation is performed by infusing citrate into the arterial line of the dialysis tubing to reduce ionized calcium concentrations in order to minimize propagation of the coagulation cascade. Ionized calcium concentrations are restored by calcium supplementation prior to reinfusion of the blood into the patient. The HepZero study suggested that regional citrate anticoagulation is superior to heparin-coated polyacrylonitrile dialyzers (AN69ST; Nephral 300ST, Gambro) and resulted in in significantly greater instantaneous urea nitrogen clearance. While generally safe and adequate, regional citrate anticoagulation requires additional actions during preparatory phase (preparation of citrate and calcium infusion pumps) as well as during the treatment (measurement of ionized calcium).

Recently, acetate-free citrate-containing dialysate concentrates were introduced into clinical practice. Besides the advantages of acetate-free dialysate, this provides a modest local anticoagulant effect inside the dialyzer. Citrate-containing dialysate allowed to reduce heparin dose while maintaining extracorporeal circuit patency and dialyzer clearance. Recently, citrate-containing dialysate and a heparin-coated dialyzer were combined. In one study, non-inferiority to regional citrate anticoagulation was demonstrated

The abovementioned studies demonstrate that hemodialysis without systemic heparinization is feasible. However, such procedures are more cumbersome, require more manpower, additional biochemical testing and/ or more expensive consumables. The aim of the current study is to test two different strategies for systemic heparin-free dialysis with an asymmetrical tri-acetate hemodialyzer.

Trial objectives To evaluate the feasability, safety and adequacy of systemic heparin-free dialysis using an asymmetrical tri-acetate dialyzer membrane, with or without the combination with citrate containing dialysate.

The main objective of the study is to test efficacy of the two study interventions to perform standard duration (i.e. 4 hours) hemodialysis without interruption due to clotting phenomena and without the use of heparin or low molecular weight heparins.

02

Conditions studied

  • Hemodialysis Complication

Keywords

  • anticoagulation
  • clotting
  • hemodialysis
  • hemodiafiltration
  • citrate
03

In context

Lead sponsor

Universitaire Ziekenhuizen KU Leuven is the lead sponsor of 928 studies on the registry; 261 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients age 18 years, or over. No maximum age is defined.
  • Providing signed and dated informed consent (ICF)
  • Maintenance dialysis (> 3 months of hemodialysis)
  • 'Standard' dialysis regimen (three dialysis sessions / week, dialysis duration 4 hours)
  • Hemodynamic stability during 4 weeks preceding study period. Hemodynamic instability is defined as any episode of low blood pressure (asymptomatic or symptomatic requiring intervention (bolus fluid infusion, temporarily withholding or reducing ultrafiltration, preterm termination of dialysis session, resuscitation)
  • Hemoglobin 9 - 12 g/dl.

Exclusion criteria

Exclusion Criteria:

  • Any known medical disorder favoring either bleeding or clotting (e.g. atypical hemolytic uremic syndrome (aHUS), antiphospholipid syndrome, idiopathic thrombocytopenic purpura (ITP), paroxysmal nocturnal hemoglobinuria (PNH))
  • Treatment with a vitamin K antagonist
  • Treatment with any one of the NOACs (apixaban, rivaroxaban, edoxaban, dabigatran)
  • High risk of bleeding according to the criteria of Swartz (12).
  • Patients with a known allergic reaction to asymmetric triacetate
  • Pregnancy
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    ATA plus citrate

    1.9 m2 ATA membrane (Solacea™-19H, Nipro Corp., Japan) in combination with citrate (1 mM) containing dialysate

    Device: dialyzer · Combination Product: hemodialysis with citrate-containing dialysate

  • Active comparator
    ATA plus predilution hemodiafiltration

    1.9 m2 ATA membrane (Solacea™-19H, Nipro Corp., Japan), in combination with high volume predilution hemodiafiltration

    Device: dialyzer · Other: predilution hemodiafiltration

Interventions

  • Devicedialyzer

    Asymmetric triacetate dialyzer

    Also known as: Solacea™-19H (Nipro Corp., Japan)

  • Combination producthemodialysis with citrate-containing dialysate

    acetate-free dialysate

    Also known as: Selectbag citrate (1mM citrate, Baxter)

  • Otherpredilution hemodiafiltration

    predilution hemodiafiltration

06

What researchers measure

Primary outcomes

  1. clinical patency of the hemodialysis extracorporeal circuit

    clotting of the extracorporeal circuit

    Time frame: 4 hours

Secondary outcomes

  1. Clotting of dialyser

    Semi-quantitative clotting score

    Time frame: 4 hours

  2. dialysis adequacy

    single pool Kt/V

    Time frame: 4hours

  3. Reduction ratio uremic retention solutes

    ratio describing the change in serum concentration over the concentration at the beginning of the dialysis session

    Time frame: 4 hours

07

Study locations

1 site
  • University Hospitals Leuven
    Leuven, Vlaams-Brabant 3000, Belgium
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 21, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04381234
Lead sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
NIPRO
Responsible party
Sponsor
First posted
May 8, 2020
Start date
Jan 6, 2018
Primary completion
Mar 10, 2019
Completion
May 5, 2020
Last update
May 21, 2020

Study contacts

bjorn D Meijers, MD, PhD
principal investigator · UZ Leuven

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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