Cardiotoxicity Clinical Trial
Official title:
Cardiac Fibrosis and Risk Prediction in Cancer Treatment-Related Cardiotoxicity
NCT number | NCT02798679 |
Other study ID # | CV-2016-24434 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | August 2016 |
Est. completion date | September 1, 2022 |
Verified date | October 2022 |
Source | University of Minnesota |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to determine whether pre-existing cardiac fibrosis is a predictor of cancer treatment-related cardiotoxicity.
Status | Completed |
Enrollment | 40 |
Est. completion date | September 1, 2022 |
Est. primary completion date | September 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 45 Years and older |
Eligibility | Inclusion Criteria: - Stage I-III breast cancer or lymphoma with a >2 year life expectancy - A treatment plan that includes anthracyclines and/or trastuzumab - Age >45 years - Able to hold breath for 10 seconds - Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 Exclusion Criteria: - Refusal or inability to provide informed consent - Known heart failure or LVEF <50% - Heart rate over 100 bpm - Renal dysfunction with GFR <30 mL/min/1.73m2 - Participants with pacemakers, defibrillators, functioning neurostimulator devices or other implanted electronic devices - Symptomatic claustrophobia - Plans to move within 24 months of enrollment |
Country | Name | City | State |
---|---|---|---|
United States | University of Minnesota | Minneapolis | Minnesota |
Lead Sponsor | Collaborator |
---|---|
University of Minnesota |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cardiotoxicity assessed clinically or by cardiac MRI | 24 months |
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