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Metabolic Aspects of Citrate Anticoagulation in Renal Replacement Therapy (Citrate)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2011 by Charles University, Czech Republic.
Recruitment status was:  Recruiting
Ministry of Health, Czech Republic
Information provided by:
Charles University, Czech Republic Identifier:
First received: May 25, 2011
Last updated: May 26, 2011
Last verified: May 2011
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.

Acute Renal Failure Critical Illness

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Metabolic Aspects of Citrate Anticoagulation in Renal Replacement Therapy

Resource links provided by NLM:

Further study details as provided by Charles University, Czech Republic:

Biospecimen Retention:   Samples Without DNA
frozen plasma

Estimated Enrollment: 120
Study Start Date: January 2008
ACD (acid-citrate-dextrose)
4% trisodium citrate
unfractionated heparin (UFH)


Ages Eligible for Study:   16 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
critically ill intensive care patients

Inclusion Criteria:

  • Acute renal failure on continuous renal replacement therapy for more than 24 hours (CVVH or CVVHDF).

Exclusion Criteria:

  • Absence of consent.
  Contacts and Locations
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Please refer to this study by its identifier: NCT01361581

Czech Republic
Dept of Anaesthesia and Intensive Care, General University Hospital, 1st Medical Faculty, Charles University Recruiting
Prague 2, Czech Republic, 120 00
Contact: Martin Balik, A/Prof   
Principal Investigator: Martin Balik, MD, PhD         
Sponsors and Collaborators
Charles University, Czech Republic
Ministry of Health, Czech Republic
  More Information

Publications automatically indexed to this study by Identifier (NCT Number):
Responsible Party: Martin Balik, A/Prof., MD, PhD, EDIC, 1st Medical Faculty, Charles University, Prague Identifier: NCT01361581     History of Changes
Other Study ID Numbers: NS/10014-4
Study First Received: May 25, 2011
Last Updated: May 26, 2011

Keywords provided by Charles University, Czech Republic:
Acute renal failure
Renal replacement therapy

Additional relevant MeSH terms:
Renal Insufficiency
Critical Illness
Acute Kidney Injury
Kidney Diseases
Urologic Diseases
Disease Attributes
Pathologic Processes
Citric Acid
Calcium Chelating Agents
Chelating Agents
Sequestering Agents
Molecular Mechanisms of Pharmacological Action processed this record on August 18, 2017