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Trials / Terminated

TerminatedNCT00195897

Early Assessment of Anthracycline-induced Cardiotoxicity (CARDIOTOX)

Early Assessment of Anthracycline-induced Cardiotoxicity: Usefulness of Biochemical Markers and Ventricular Function Assessment.

Status
Terminated
Phase
Study type
Observational
Enrollment
6 (actual)
Sponsor
Centre Henri Becquerel · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Anthracycline-based chemotherapy is a key point of the treatment of patients with Hodgkin's and non-Hodgkin's lymphomas. However, cumulative doses are limited by cardiotoxicity, resulting in a marked left ventricular function impairment that may lead to heart failure. The standard clinical approach to monitoring for anthracycline cardiotoxicity is based on cardiac function monitoring using echocardiography or radionuclide angiography. The aim of this study is to evaluate the usefulness of biochemical markers of cardiac injury (troponin and NT-proBNP) and structural changes on cardiac MR in predicting anthracycline cardiotoxicity.

Conditions

Timeline

Start date
2006-01-01
Primary completion
2009-12-01
Completion
2009-12-01
First posted
2005-09-20
Last updated
2016-08-22

Locations

2 sites across 1 country: France

Source: ClinicalTrials.gov record NCT00195897. Inclusion in this directory is not an endorsement.

Early Assessment of Anthracycline-induced Cardiotoxicity (CARDIOTOX) (NCT00195897) · Clinical Trials Directory