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Assessment of Electrolyte Values in the Intensive Care Unit:Comparison Between Arterial and Venous Blood Gas Analysis and Formal Laboratory Testing

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ClinicalTrials.gov Identifier: NCT00256061
Recruitment Status : Withdrawn (Due to the publication of significant literature in this area since commencement of the project which has now rendered the project unnecessary.)
First Posted : November 21, 2005
Last Update Posted : April 27, 2015
Sponsor:
Information provided by:
Melbourne Health

Brief Summary:
The study hypothesis is that in critically ill patients there is significant differences between electrolyte levels measured using blood gas analysers and by laboratory techniques, and between levels measured on arterial and venous blood samples.

Condition or disease
Electrolyte Values

Detailed Description:

The sudy hypothesis is that in critically ill patients there is a significant difference between electrolyte levels measured using blood gas analysers and by laboratory techniques, and between levels measured on arterial and venous blood samples.

The study aim is determine the agreement between electrolyte levels measure by formal laboratory serum analysis and point-of-care blood gas analysis.

Also, to determine the agreement between electrolyte levels measured on simultaneous arterial and venous blood samples, using both serum and whole blood samples.


Study Type : Observational
Actual Enrollment : 0 participants
Time Perspective: Retrospective
Official Title: Assessment of Electrolyte Values in the Intensive Care Unit:Comparison Between Arterial and Venous Blood Gas Analysis and Formal Laboratory Testing
Study Start Date : February 2003
Study Completion Date : February 2004




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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Adult patients 18 years or older admitted to the intensive care unit
  2. Patients who have arterial and central venous access insitu for clinical management purposes.
  3. Patients who consent to inclusion in the study, or if the patient is not competent, the next of kins' consent.

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00256061


Sponsors and Collaborators
Melbourne Health
Investigators
Principal Investigator: Megan Robertson, MBBS Royal Melbourne Hospital, Intensive Care Unit

ClinicalTrials.gov Identifier: NCT00256061     History of Changes
Other Study ID Numbers: 2002.229
First Posted: November 21, 2005    Key Record Dates
Last Update Posted: April 27, 2015
Last Verified: April 2015