A Trial Testing Amiodarone in Chagas Cardiomiopathy

Chagas Cardiomyopathy Clinical Trial

— ATTACH  

Official title:

A Trial Testing Amiodarone in Chagas Cardiomyopathy (ATTACH)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03193749
• Other study ID #: 880-2015
• Secondary ID: 277872553480
• Status: Recruiting
• Phase: Phase 3
• First received: June 19, 2017
• Last updated: June 20, 2017
• Start date: June 12, 2017
• Est. completion date: December 2020

Study information

• Verified date: June 2017
• Source: Fundación Cardioinfantil Instituto de Cardiología
• Contact: Juan C Villar, MD, MSc, PhD
• Phone: 16672727
• Email: jvillarc[@]cardioinfantil.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: December 2020
• Est. primary completion date: June 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

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

1. 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

2. 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

Related Conditions & MeSH terms

• Cardiomyopathies
• Chagas Cardiomyopathy

Intervention

Drug:
• Amiodarone Hydrochloride
Starting (loading) dose 400 mg PO once a day for 10 days. Maintainance dose 200 mg PO once a day for at least 6 months, up to 24 months
• Placebo Oral Tablet
Matching placebo for tablets of 200 mg of Amiodarone

Locations

Country	Name	City	State
Colombia	Fundación Cardioinfantil - Instituto de Cardiología	Bogotá

Sponsors (2)

Lead Sponsor	Collaborator
Fundación Cardioinfantil Instituto de Cardiología	Instituto de Corazón de Bucaramanga

Country where clinical trial is conducted

Colombia, 

References & Publications (5)

Adesse D, Azzam EM, Meirelles Mde N, Urbina JA, Garzoni LR. Amiodarone inhibits Trypanosoma cruzi infection and promotes cardiac cell recovery with gap junction and cytoskeleton reassembly in vitro. Antimicrob Agents Chemother. 2011 Jan;55(1):203-10. doi: 10.1128/AAC.01129-10. Epub 2010 Nov 15. — View Citation

Benaim G, Sanders JM, Garcia-Marchán Y, Colina C, Lira R, Caldera AR, Payares G, Sanoja C, Burgos JM, Leon-Rossell A, Concepcion JL, Schijman AG, Levin M, Oldfield E, Urbina JA. Amiodarone has intrinsic anti-Trypanosoma cruzi activity and acts synergistically with posaconazole. J Med Chem. 2006 Feb 9;49(3):892-9. — View Citation

Rassi A Jr, Rassi A, Little WC, Xavier SS, Rassi SG, Rassi AG, Rassi GG, Hasslocher-Moreno A, Sousa AS, Scanavacca MI. Development and validation of a risk score for predicting death in Chagas' heart disease. N Engl J Med. 2006 Aug 24;355(8):799-808. — View Citation

Rassi A Jr, Rassi A, Rassi SG. Predictors of mortality in chronic Chagas disease: a systematic review of observational studies. Circulation. 2007 Mar 6;115(9):1101-8. Review. — View Citation

Veiga-Santos P, Barrias ES, Santos JF, de Barros Moreira TL, de Carvalho TM, Urbina JA, de Souza W. Effects of amiodarone and posaconazole on the growth and ultrastructure of Trypanosoma cruzi. Int J Antimicrob Agents. 2012 Jul;40(1):61-71. doi: 10.1016/j.ijantimicag.2012.03.009. Epub 2012 May 14. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Positive PCR for Trypanosoma cruzi	Conventional (qualitative) Polymerase Chain Reaction. At least one positive result out of three tests at least one week apart from each other	6 months after starting treatment
Secondary	Composite of clinical events	a) All-cause deaths; b) EKG-supported ventricular tachycardia or, c) Hospitalization for cardiac causes	Up to study closure or 24 months after randomization (whichever comes first)
Secondary	Elements of the composite outcome of clinical events individually		Up to study closure or 24 months after randomization (whichever comes first)