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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03191162
Other study ID # 2016-003789-21
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date April 21, 2017
Est. completion date March 16, 2021

Study information

Verified date December 2023
Source Hospital Universitari Vall d'Hebron Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A phase 2 clinical trial to evaluate the the efficacy of different benznidazole regimens (300mg/day for 60 days, 150mg/day for 60 days, and 400mg/day for 15 days) for the treatment of chronic Chagas disease in adult patients. The efficacy is assessed through the proportion of patients with negative parasitaemia measured by Polymerase Chain Reaction (PCR) during the first 12 months after starting treatment. The study will be performed in Spain, Brazil, Argentina and Colombia.


Recruitment information / eligibility

Status Completed
Enrollment 238
Est. completion date March 16, 2021
Est. primary completion date September 21, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Over 18 years old. - Diagnosis of Chagas disease through two different serological tests. - Positive T. cruzi PCR in peripheral blood. - Signed informed consent. Exclusion Criteria: - Previous treatment with Benznidazole or Nifurtimox. - Alcohol consumption. - Acute or chronic health problems that could interfere in the assessment of the efficacy or safety of the drug (acute infections, HIV infection, liver or renal impairment, etc). - Nitroimidazole hipersensitivity. - Concomitant or previous treatment with allopurinol or antifungal drugs. - Pregnancy.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Benznidazole
To evaluate different regimens of Benznidazole for the treatment of chronic Chagas disease

Locations

Country Name City State
Argentina Instituto Nacional de Parasitología Dr. Mario Fatala Chaben (ANLIS) Buenos Aires
Argentina Instituto de Cardiología de Corrientes Juana Francisca Cabral Corrientes
Brazil Centro de Pesquisas René Rachou - Fundação Oswaldo Cruz. (FIOCRUZ) Belo Horizonte
Brazil Hospital Universitário Clemente de Faria Montes Claros
Colombia Fundación Cardioinfantil - Instituto de Cardiología Bogotá
Colombia Centro Atencion y Diagnóstico de Enfermedades Infecciosas Bucaramanga
Spain Infectious Disease Department Vall d'Hebron Hospital Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Hospital Universitari Vall d'Hebron Research Institute

Countries where clinical trial is conducted

Argentina,  Brazil,  Colombia,  Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of patients with negative parasitaemia measured by PCR during the first 12 months after starting treatment The treatment efficacy is assessed through the proportion of patients with negative parasitaemia measured by PCR during the first 12 months after starting treatment 12 months
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