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NCT01639313 Clinical Trial

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

Cardiac Diseases Clinical Trial

Official title:
Is Arterial Pulse Contour Analysis Using Nexfin a New Option in the Non-invasive Measurement of Cardiac Output? - A Pilot Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01639313
Other study ID # PCA_CMR_MA
Secondary ID
Status Completed
Phase N/A
First received July 9, 2012
Last updated July 9, 2012
Start date June 2011
Est. completion date November 2011

Study information
Verified date July 2012
Source Universitätsmedizin Mannheim
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial 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).

Recruitment information / eligibility
Status Completed
Enrollment 39
Est. completion date November 2011
Est. primary completion date November 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- indication for CMR

Exclusion Criteria:

- contraindication for CMR

- claustrophobia

- no consent obtained

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Germany Universitätsmedizin Mannheim Mannheim

Sponsors (1)
Lead Sponsor Collaborator
Universitätsmedizin Mannheim

Country where clinical trial is conducted

Germany, 

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