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.