Skip to main content
OpenTrials
Completed

NCT Number: NCT00752453

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

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)

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Includes ICU patients with lactate acidosis with acute renal failure

Exclusion criteria

Treatment and study plan

Dialysis during 4 hours

Procedure

Blood and dialysate sampling

Dialysis during 6 hours

Procedure

Blood and dialysate sampling

Dialysis during 8 hours

Procedure

Blood and dialysate sampling

Primary outcomes

  1. Toxin removal

    Time frame: During dialysis

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Registry information

Official study 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

Important dates

Study start
2008
Primary completion
2013
Study completion
2013
First posted
Sep 15, 2008
Registry last updated
Dec 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.