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Sponsored by: |
University Hospital, Ghent |
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Information provided by: | University Hospital, Ghent |
ClinicalTrials.gov Identifier: | NCT00148044 |
Determination of the concentration of uremic toxins of sepsis patients with or without acute kidney failure compared to the concentrations of uremic toxins of chronically uremic patients
Condition | Intervention |
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Kidney Failure, Acute |
Procedure: Blood sampling for determination of uremic toxins |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | Uremic Toxins of Patients With Acute Kidney Failure |
Estimated Enrollment: | 30 |
Study Start Date: | October 2003 |
Study Completion Date: | February 2004 |
Determination of the concentration of uremic toxins of sepsis patients with or without acute kidney failure compared to the concentrations of uremic toxins of chronically uremic patients
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | 2003/298 |
Study First Received: | September 6, 2005 |
Last Updated: | December 19, 2007 |
ClinicalTrials.gov Identifier: | NCT00148044 |
Health Authority: | Belgium: Institutional Review Board |
Renal Insufficiency Urologic Diseases Renal Insufficiency, Acute |
Kidney Diseases Kidney Failure, Acute Kidney Failure |