Haemodialysis Clinical Trial
Official title:
Uremic Toxin Removal With a New High Flux Cellulose Triacetate Membrane
Verified date | December 2007 |
Source | University Hospital, Ghent |
Contact | n/a |
Is FDA regulated | No |
Health authority | Belgium: Institutional Review Board |
Study type | Interventional |
Comparison of the uremic toxin removal by haemodialysis either with a low flux or a new high flux cellulose triacetate membrane
Status | Completed |
Enrollment | 12 |
Est. completion date | April 2002 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Chronic haemodialysis patient - Serum albumin > 3.6 g/dl Exclusion Criteria: - < 18 years |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Belgium | University Hospital Ghent | Ghent |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Ghent | Nissho Nipro Europe |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Concentration of uremic components after 3 weeks of haemodialysis |
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