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Correspondence of ScO2 and Cardiac Output in Hemodialysis

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 October 2010 by Danish State Hospital.
Recruitment status was:  Recruiting
ClinicalTrials.gov Identifier:
First Posted: December 3, 2010
Last Update Posted: October 12, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Danish State Hospital
The study aims to investigate the correspondence between changes in central venous oxygen saturation (ScO2) and in cardiac output during hemodialysis. In 12 hemodialysis patients with an A-V fistula, a thoracic bioimpedance cardiograph will be validated for cardiac output measurements during ongoing hemodialysis. Provided this validation is satisfactory, impedance cardiography cardiac output and ScO2 will be measured at intervals during hemodialysis in 25 hemodialysis patients with a central vascular access. Absolute values and trends will be compared.


Study Type: Observational
Official Title: ScO2 and Cardiac Output - Correspondence Study in Hemodialysis Patients

Resource links provided by NLM:

Further study details as provided by Danish State Hospital:

Estimated Enrollment: 37
Study Start Date: November 2010
Estimated Study Completion Date: November 2011
Estimated Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)
Hemodialysis patients


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Hemodialysis patients

Inclusion Criteria:

Ambulatory hemodialysis patients in the Copenhagen University Hospital department of Nephrology.

Exclusion Criteria:

Age below 18 years. Failure to give informed consent.

  Contacts and Locations
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): NCT01252394

Contact: Joakim Cordtz, MD +45 60 85 93 96 drcordtz@yahoo.dk

Copenhagen University Hospital Recruiting
Copenhagen E, Denmark, 2100
Principal Investigator: Joakim Cordtz, MD         
Sponsors and Collaborators
Danish State Hospital
Study Director: Soeren D Ladefoged, MD Dep. of Nephrology, Copenhagen University Hospital.
  More Information

Responsible Party: Joakim Cordtz/MD, Department of Nephrology, Copenhagen University Hospital
ClinicalTrials.gov Identifier: NCT01252394     History of Changes
Other Study ID Numbers: ScO2 cardiac output
First Submitted: December 2, 2010
First Posted: December 3, 2010
Last Update Posted: October 12, 2017
Last Verified: October 2010