Critical Illness Clinical Trial
— CitrateOfficial title:
Metabolic Aspects of Citrate Anticoagulation in Renal Replacement Therapy
NCT number | NCT01361581 |
Other study ID # | NS/10014-4 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | May 25, 2011 |
Last updated | May 26, 2011 |
Start date | January 2008 |
Verified date | May 2011 |
Source | Charles University, Czech Republic |
Contact | n/a |
Is FDA regulated | No |
Health authority | Czech Republic: Ethics Committee |
Study type | Observational |
Citrate anticoagulation is associated with metabolic side effects which are linked to a portion of citrate reaching systemic circulation. Data on significance of systemic gain of citrate and its relationship to method configuration are missing. Patient might also receive certain dose of lactate as a buffer and a dose of glucose if acid-citrate-dextrose solution is used. The authors test variable methods of indirect estimate of systemic dose of citrate which would allow to quantify the metabolic input without mostly unavailable measurements of citrate levels.
Status | Recruiting |
Enrollment | 120 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 16 Years and older |
Eligibility |
Inclusion Criteria: - Acute renal failure on continuous renal replacement therapy for more than 24 hours (CVVH or CVVHDF). Exclusion Criteria: - Absence of consent. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Czech Republic | Dept of Anaesthesia and Intensive Care, General University Hospital, 1st Medical Faculty, Charles University | Prague 2 |
Lead Sponsor | Collaborator |
---|---|
Charles University, Czech Republic | Ministry of Health, Czech Republic |
Czech Republic,
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