Chagas Cardiomyopathy Clinical Trial
Official title:
A Trial Testing Amiodarone in Chagas Cardiomyopathy (ATTACH)
Purpose:
The ATTACH trial, as currently designed, will primarily test whether a treatment with
Amiodarone for at least 6 months has a trypanocidal effect among individuals with
mild-to-moderate Chronic Chagas Cardiomyopathy. A secondary goal will be to confirm, in this
population, a clinical benefit from this treatment (in terms of reducing mortality or
cardiac arrhythmic events), and to explore whether a potential trypanocidal effect is
associated with a clinical benefit.
Investigators currently plan to enroll over 200 participants in Bogotá and Bucaramanga,
Colombia. Such sample size will provide 82% of statistical power to detect at least a 30%
relative reduction in the primary outcome. This is assuming that at least 75% of untreated
participants will test positive at least once after three qualitative PCR assays for
Trypanosoma cruzi during the 6th month after randomization (allowing for up to 10% losses to
follow up and treatment adherence over 90%).
ATTACH is currently seeking collaborating centers internationally. The current funding
structure will allow to test study hypothesis on trypanocidal effect, whereas data on
clinical effects will be exploratory. Investigators expect to increase the sample size to at
least 600 participants in order to a) enhance geographical variability/generalizability for
the primary results and b) to achieve enough statistical power to test the hypothesis on
clinical impact.
New centers are welcome to join this protocol, either as a placebo-controlled or as a
pragmatic, open label trial. These centers will be working with the central coordination
with their own funding/logistic capabilities. In the open label protocol, eligible,
consenting participants will be randomly prescribed or not to Amiodarone. As assessing
clinical impact will be the priority, new centers are not required to have on-site PCR
capabilities. These centers are encouraged to store blood samples for PCR testing elsewhere
later, if possible.
See details on eligibility, interventions and outcome measures below
;
Status | Clinical Trial | Phase | |
---|---|---|---|
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