ClinicalTrials.Veeva

Menu

Elimination of Protein-bound Uremic Retention Solutes by Prometheus Artificial Hepatic System Versus Conventional Dialysis

G

Ghent University Hospital (UZ)

Status

Withdrawn

Conditions

Renal Failure, Chronic

Treatments

Device: Dialysis with different artificial devices

Study type

Interventional

Funder types

Other

Identifiers

NCT00262353
2004/416

Details and patient eligibility

About

Comparison of the efficacy of dialysis by conventional dialysis versus Prometheus artificial hepatic system

Full description

After inclusion, patients will be dialysed with low-flux artificial kidneys. 1 week of dialysis exists of 3 days of dialysis. In week 4, day 2, patients will be treated once with the Prometheus artificial hepatic system or with high-flux dialysis. The other days low-flux kidneys will be used. Week 5 and 6 are a wash-out period. Week 7 is identical to week 4 but the other system than in week 4 is used. Blood samples are taken at regular moments in week 3, week 4 (day 2) and week 7 (day 2).

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Stable patients
  • At least 3 months on dialysis
  • Arterio-venous fistula

Exclusion criteria

  • Diabetic patients
  • Malignancies
  • Acute illnesses

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems