Heart Failure Clinical Trial
Official title:
Early Detection of Cardiac Toxicity in Childhood Cancer Survivors
NCT number | NCT03038997 |
Other study ID # | 5405 |
Secondary ID | |
Status | Terminated |
Phase | |
First received | |
Last updated | |
Start date | November 2014 |
Est. completion date | March 11, 2018 |
Verified date | November 2018 |
Source | Children's Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
To evaluate cardiac MRI and/or serum biomarkers for detecting cardiac cardiac toxicity in children who received anthracycline based chemotherapy (ABC).
Status | Terminated |
Enrollment | 42 |
Est. completion date | March 11, 2018 |
Est. primary completion date | March 11, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 8 Years to 25 Years |
Eligibility |
Inclusion Criteria: - Subjects that have received anthracycline based chemotherapy - Age: 8 years old - 25 years old - Subjects that do not require sedation for cardiac MRI. - Subjects must have completed treatment in the last 10 years Exclusion Criteria: - Patients with significant congenital heart defects - Patients with renal injury or renal failure, defined as an estimated glomerular filtration rate [eGFR] <30 ml/min/1.73 m2 body surface area), as previously calculated) - Patients that require sedation for a cardiac MRI - Subjects that are pregnant or lactating - Patients with contraindications to a cardiac MRI: - Cardiac pacemaker or implantable defibrillator - Cerebral aneurysm clip - Neural stimulator - Metallic ocular foreign body - Any implanted device (i.e. insulin pump, drug infusion device) - Claustrophobia - Metal shrapnel or bullet - Investigator assessment of inability to comply with protocol - Unable/unwilling to lie still throughout the research procedure - Persons with cognitive impairment |
Country | Name | City | State |
---|---|---|---|
United States | Children's National Health System | Washington | District of Columbia |
Lead Sponsor | Collaborator |
---|---|
Niti Dham |
United States,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Echocardiogram marker measurements pre ABC chemo and post ABC | •Measure echocardiogram markers on pre anthracycline based chemotherapy (ABC) and post ABC echocardiograms, using standard echocardiogram measurements and speckle tracking. | At the end of each cardiac MRI exam through study completion, up to 5 years | |
Secondary | Detection of cardiac toxicity on MRI and echocardiogram | •Measure sensitivity of detecting cardiac toxicity between standard echocardiogram, speckle tracking on echo, and MRI | At the end of each cardiac MRI exam through study completion, up to 5 years | |
Secondary | Serum biomarkers correlation | •Correlate measurement of serum biomarkers with prevalence of cardiac changes measured on echocardiograms and MRI imaging. | At the end of the study, up to 10 years |
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