Early Detection of Cardiac Toxicity in Childhood Cancer Survivors
Stopped early
Conditions studied: Heart Failure, Cardiotoxicity
In brief
To evaluate cardiac MRI and/or serum biomarkers for detecting cardiac cardiac toxicity in children who received anthracycline based chemotherapy (ABC).
Key facts
- Study ID
- NCT03038997
- Run by
- Niti Dham
- People needed
- 42
- Starts
- 2014-11-01
- Expected to finish
- 2018-03-11
- Last updated by the study team
- 2018-12-04
Who can join
Age: 8 and older, up to 25. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Children's National Health System — Washington D.C., District of Columbia, United States
Full record on ClinicalTrials.gov
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