Comparison of Nexfin Pulse Contour Analysis and Cardiac Magnetic Resonance Imaging for the Measurement of Cardiac Output

This study has been completed.

Sponsor:

Information provided by (Responsible Party):

Joachim Saur, University Hospital Mannheim

ClinicalTrials.gov Identifier:

NCT01639313

First received: July 9, 2012

Last updated: NA

Last verified: July 2012

History: No changes posted

Tracking Information
First Received Date ^ICMJE	July 9, 2012
Last Updated Date	July 9, 2012
Start Date ^ICMJE	June 2011
Primary Completion Date	November 2011 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE
Original Primary Outcome Measures ^ICMJE
Change History	No Changes Posted
Current Secondary Outcome Measures ^ICMJE
Original Secondary Outcome Measures ^ICMJE
Current Other Outcome Measures ^ICMJE
Original Other Outcome Measures ^ICMJE

Descriptive Information
Brief Title ^ICMJE	Comparison of Nexfin Pulse Contour Analysis and Cardiac Magnetic Resonance Imaging for the Measurement of Cardiac Output
Official Title ^ICMJE	Is Arterial Pulse Contour Analysis Using Nexfin a New Option in the Non-invasive Measurement of Cardiac Output? - A Pilot Study
Brief Summary	A growing interest in monitoring cardiac output (CO) non-invasively has emerged, however its determination has been difficult using the standard approaches. The aim of the study is to evaluate the accuracy and precision of pulse contour analysis (PCA) as compared to cardiac magnetic resonance imaging (CMR).
Detailed Description
Study Type ^ICMJE	Observational
Study Design ^ICMJE	Observational Model: Cohort Time Perspective: Prospective
Biospecimen
Sampling Method	Probability Sample
Study Population	Hemodynamically stable patients undergoing CMR
Condition ^ICMJE	Cardiac Diseases
Intervention ^ICMJE
Study Group/Cohort (s)
Publications *
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Completed
Enrollment ^ICMJE	39
Completion Date	November 2011
Primary Completion Date	November 2011 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	Inclusion Criteria: indication for CMR Exclusion Criteria: contraindication for CMR claustrophobia no consent obtained
Gender	Both
Ages	18 Years and older
Accepts Healthy Volunteers	No
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	Germany

Administrative Information
NCT Number ^ICMJE	NCT01639313
Other Study ID Numbers ^ICMJE	PCA_CMR_MA
Has Data Monitoring Committee
Responsible Party	Joachim Saur, University Hospital Mannheim
Study Sponsor ^ICMJE	University Hospital Mannheim
Collaborators ^ICMJE
Investigators ^ICMJE
Information Provided By	University Hospital Mannheim
Verification Date	July 2012
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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