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Clinical Trials/NCT00541801
NCT00541801
Completed
Not Applicable

Acoustic Cardiographic Assessment of Heart Function in Comparison to Doppler-echocardiography in Patients With Cytostatic Therapies

Luzerner Kantonsspital1 site in 1 countryMarch 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure, Congestive
Sponsor
Luzerner Kantonsspital
Locations
1
Primary Endpoint
Changes of echocardiographic parameters and changes of electromechanical activation time (EMAT)and development of third heart sound as indicators of congestive heart failure
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

In this study, the investigators sought to determine whether an acoustic cardiographic assessment of heart function is equivalent to Doppler-echocardiography in patients who are treated with cardio-toxic cytostatic agents.

Detailed Description

Patients receiving cardio-toxic cytostatic agents are examined by Doppler-echocardiography and acoustic cardiography before, during, and after the cytostatic treatment. Doppler-echocardiography measures ejection fraction, TDI, speckle tracking, and further parameters. Acoustic cardiography (Audicor, Inovise Medical Inc., Portland, USA) simultaneously integrates heart sounds and single-channel electrocardiography input to generate multiple parameters that correlate to established hemodynamic measures. Heart function as assessed by Doppler-echocardiography is then compared to the heart function as assessed by Audicor ECG.

Registry
clinicaltrials.gov
Start Date
March 2007
End Date
June 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients with malignant disease with scheduled anthracycline and trastuzumab therapy

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Changes of echocardiographic parameters and changes of electromechanical activation time (EMAT)and development of third heart sound as indicators of congestive heart failure

Time Frame: Repeated measurements over a year

Secondary Outcomes

  • Development of clinically overt congestive heart failure(One year)

Study Sites (1)

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