Uremic Toxins of Patients With Acute Kidney Failure
This study has been completed.
Sponsor:
University Hospital, Ghent
Information provided by:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00148044
First received: September 6, 2005
Last updated: December 19, 2007
Last verified: December 2007
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Purpose
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 |
|---|---|
|
Kidney Failure, Acute |
Procedure: Blood sampling for determination of uremic toxins |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Uremic Toxins of Patients With Acute Kidney Failure |
Further study details as provided by University Hospital, Ghent:
| 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
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Intensive Care patients with sepsis
- Patients with acute kidney failure: serum creatinin > 2 mg/dl
- Chronic haemodialysis patients
Exclusion Criteria:
- < 18 years
Contacts and Locations
More Information
Additional Information:
No publications provided
| ClinicalTrials.gov Identifier: | NCT00148044 History of Changes |
| Other Study ID Numbers: | 2003/298 |
| Study First Received: | September 6, 2005 |
| Last Updated: | December 19, 2007 |
| Health Authority: | Belgium: Institutional Review Board |
Additional relevant MeSH terms:
|
Acute Kidney Injury Renal Insufficiency Kidney Diseases Urologic Diseases |
ClinicalTrials.gov processed this record on May 16, 2013