Uremic Toxin Removal With a New High Flux Cellulose Triacetate Membrane
This study has been completed.
Sponsor:
University Hospital, Ghent
Collaborator:
Nissho Nipro Europe
Information provided by:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00230906
First received: September 29, 2005
Last updated: December 19, 2007
Last verified: December 2007
| Tracking Information | |||||
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| First Received Date ICMJE | September 29, 2005 | ||||
| Last Updated Date | December 19, 2007 | ||||
| Start Date ICMJE | January 2001 | ||||
| Primary Completion Date | Not Provided | ||||
| Current Primary Outcome Measures ICMJE |
Concentration of uremic components after 3 weeks of haemodialysis | ||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT00230906 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Uremic Toxin Removal With a New High Flux Cellulose Triacetate Membrane | ||||
| Official Title ICMJE | Uremic Toxin Removal With a New High Flux Cellulose Triacetate Membrane | ||||
| Brief Summary | Comparison of the uremic toxin removal by haemodialysis either with a low flux or a new high flux cellulose triacetate membrane |
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| Detailed Description | Comparison of the uremic toxin removal by haemodialysis either with a low flux or a new high flux cellulose triacetate membrane |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Treatment |
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| Condition ICMJE | Haemodialysis | ||||
| Intervention ICMJE | Procedure: Haemodialysis with either low or high flux membranes | ||||
| Study Arm (s) | Not Provided | ||||
| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 12 | ||||
| Completion Date | April 2002 | ||||
| Primary Completion Date | Not Provided | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Belgium | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00230906 | ||||
| Other Study ID Numbers ICMJE | 2001/182 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Not Provided | ||||
| Study Sponsor ICMJE | University Hospital, Ghent | ||||
| Collaborators ICMJE | Nissho Nipro Europe | ||||
| Investigators ICMJE |
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| Information Provided By | University Hospital, Ghent | ||||
| Verification Date | December 2007 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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