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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00230906
Other study ID # 2001/182
Secondary ID
Status Completed
Phase N/A
First received September 29, 2005
Last updated December 19, 2007
Start date January 2001
Est. completion date April 2002

Study information

Verified date December 2007
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Comparison of the uremic toxin removal by haemodialysis either with a low flux or a new high flux cellulose triacetate membrane


Description:

Comparison of the uremic toxin removal by haemodialysis either with a low flux or a new high flux cellulose triacetate membrane


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Haemodialysis with either low or high flux membranes


Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Ghent Nissho Nipro Europe

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Concentration of uremic components after 3 weeks of haemodialysis
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