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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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9 January 2023 |
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Main ID: |
NCT00752453 |
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Date of registration:
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12/09/2008 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Uremic Toxins in the Intensive Care Units (ICU): Patients With Lactate Acidosis
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Scientific title:
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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 |
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Date of first enrolment:
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July 31, 2008 |
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Target sample size:
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8 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT00752453 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Belgium
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Contacts
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Name:
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Raymond Vanholder, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University Hospital, Ghent |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Includes ICU patients with lactate acidosis with acute renal failure
Exclusion Criteria:
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Acute Renal Failure
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Intervention(s)
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Procedure: Dialysis during 4 hours
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Procedure: Dialysis during 6 hours
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Procedure: Dialysis during 8 hours
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Primary Outcome(s)
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Toxin removal
[Time Frame: During dialysis]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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