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NCT00148044 Clinical Trial

Uremic Toxins of Patients With Acute Kidney Failure

Kidney Failure, Acute Clinical Trial

Official title:
Uremic Toxins of Patients With Acute Kidney Failure

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00148044
Other study ID # 2003/298
Secondary ID
Status Completed
Phase N/A
First received September 6, 2005
Last updated December 19, 2007
Start date October 2003
Est. completion date February 2004

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 Observational

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date February 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Intensive Care patients with sepsis

- Patients with acute kidney failure: serum creatinin > 2 mg/dl

- Chronic haemodialysis patients

Exclusion Criteria:

- < 18 years

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• Blood sampling for determination of uremic toxins

Locations
Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

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