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NCT00752453 Clinical Trial

Uremic Toxins in the Intensive Care Units (ICU): Patients With Lactate Acidosis

Acute Renal Failure Clinical Trial

Official title:
Study of the Kinetics of Uremic Toxins in the ICU Patients With Acute Renal Failure, in Order to Optimize the Dialysis Dose: Patients With Lactate Acidosis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00752453
Other study ID # 2008/375
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 31, 2008
Est. completion date December 31, 2013

Study information
Verified date December 2022
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study of the kinetics of uremic toxins in the ICU patients with acute renal failure, in order to optimize the dialysis dose: patients with lactate acidosis. The sampling of blood and dialysate will be done during dialysis with different durations (4, 6 and 8 h)

Recruitment information / eligibility
Status Completed
Enrollment 8
Est. completion date December 31, 2013
Est. primary completion date October 4, 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Includes ICU patients with lactate acidosis with acute renal failure Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Dialysis during 4 hours
Blood and dialysate sampling
• Dialysis during 6 hours
Blood and dialysate sampling
• Dialysis during 8 hours
Blood and dialysate sampling

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, 

Outcome
Type Measure Description Time frame Safety issue
Primary Toxin removal During dialysis
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