A Trial Testing Amiodarone in Chagas Cardiomiopathy (ATTACH)
Chagas Cardiomyopathy
About this trial
This is an interventional treatment trial for Chagas Cardiomyopathy focused on measuring Chagas disease, cardiomyopathy, amiodarone, clinical trial
Eligibility Criteria
ATTACH will enroll individuals with positive serology for Trypanozoma cruzi and evidence of both structrural and rythm/conduction cardiac abnormalities, as defined by any of the following inclusion criteria
Structural cardiac abnormality (at least one):
- NTpro-BNP values >125 ng/ml, or BNP values > 50 ng/ml
- Left ventricular ejection fraction (LVEF) <50% or left diastolic diameter > 5.5 cm
- Symptoms of heart failure, or one episode of acute heart failure over the last 12 months
Rrythm/conduction cardiac abnormality (at least one)
- EKG monitoring showing 10 or more VPBs/hour or ventricular Tachycardia
- EKG showing left anterior hemiblockade or right bundle branch blocakde
- Use of a cardiac stimulation device as treatment for A-V block or Sinus node dysfunction
The protocol allows concurrent treatments for the condition (e.g. beta-blockers, ACE inhibitors, etc.) other than Amiodarone. Individuals meeting the above eligibility criteria who have previously received trypanocidal therapy (e.g. Benznidazole or Nifurtimox) can still be included, as long as they prove to be PCR positive for T. cruzi at enrollment. Co-intervention with these agents during the study will also be allowed, as per physician's judgment, either as open label treatment, or as part of another study not involving Amiodarone.
Exclusion criteria:
- LVEF < 30% or NYHA Class III-IV
- Medical prescription with chronic use of Amiodarone
- Pregancy (currently, or planned in the following 2 years), or childbearing age without reliable birth control
- Heart rate < 50 or AV blockade without treatment with cardiac stimulation device
- Contraindication for Amiodarone as per treating physician (e.g. because of long QT syndrome, thyroid disease, interstitial lung disease)
- Atrial fibrillation
Sites / Locations
- Fundación Cardioinfantil - Instituto de CardiologíaRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Amiodarone Hydrochloride
Placebo
Oral treatment for at least 6 months
Oral treatment for at least 6 months