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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