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Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study

BACKGROUND: Cardiovascular diseases are the major cause of death in the world. Current treatments have not been able to reverse this scenario, creating the need for the development of new therapies. Cell therapies have emerged as an alternative for cardiac diseases of distinct causes in experimental...

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Autores principales: Tura, Bernardo R, Martino, Helena F, Gowdak, Luis H, dos Santos, Ricardo Ribeiro, Dohmann, Hans F, Krieger, José E, Feitosa, Gilson, Vilas-Boas, Fábio, Oliveira, Sérgio A, Silva, Suzana A, Bozza, Augusto Z, Borojevic, Radovan, de Carvalho, Antonio C Campos
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1783861/
https://www.ncbi.nlm.nih.gov/pubmed/17233910
http://dx.doi.org/10.1186/1745-6215-8-2
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author Tura, Bernardo R
Martino, Helena F
Gowdak, Luis H
dos Santos, Ricardo Ribeiro
Dohmann, Hans F
Krieger, José E
Feitosa, Gilson
Vilas-Boas, Fábio
Oliveira, Sérgio A
Silva, Suzana A
Bozza, Augusto Z
Borojevic, Radovan
de Carvalho, Antonio C Campos
author_facet Tura, Bernardo R
Martino, Helena F
Gowdak, Luis H
dos Santos, Ricardo Ribeiro
Dohmann, Hans F
Krieger, José E
Feitosa, Gilson
Vilas-Boas, Fábio
Oliveira, Sérgio A
Silva, Suzana A
Bozza, Augusto Z
Borojevic, Radovan
de Carvalho, Antonio C Campos
author_sort Tura, Bernardo R
collection PubMed
description BACKGROUND: Cardiovascular diseases are the major cause of death in the world. Current treatments have not been able to reverse this scenario, creating the need for the development of new therapies. Cell therapies have emerged as an alternative for cardiac diseases of distinct causes in experimental animal studies and more recently in clinical trials. METHOD/DESIGN: We have designed clinical trials to test for the efficacy of autologous bone marrow derived mononuclear cell therapies in four different cardiopathies: acute and chronic ischemic heart disease, and Chagasic and dilated cardiomyopathy. All trials are multicenter, randomized, double-blind and placebo controlled. In each trial 300 patients will be enrolled and receive optimized therapy for their specific condition. Additionally, half of the patients will receive the autologous bone marrow cells while the other half will receive placebo (saline with 5% autologous serum). For each trial there are specific inclusion and exclusion criteria and the method for cell delivery is intramyocardial for the chronic ischemic heart disease and intracoronary for all others. Primary endpoint for all studies will be the difference in ejection fraction (determined by Simpson's rule) six and twelve months after intervention in relation to the basal ejection fraction. The main hypothesis of this study is that the patients who receive the autologous bone-marrow stem cell implant will have after a 6 month follow-up a mean increase of 5% in absolute left ventricular ejection fraction in comparison with the control group. DISCUSSION: Many phase I clinical trials using cell therapy for cardiac diseases have already been performed. The few randomized studies have yielded conflicting results, rendering necessary larger well controlled trials to test for efficacy of cell therapies in cardiopathies. The trials registration numbers at the NIH registry are the following: Chagasic cardiomyopathy (NCT00349271), dilated cardiomyopathy (NCT00333827), acute myocardial infarction (NCT00350766) and Chronic Ischemic Heart Disease (NCT00362388).
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spelling pubmed-17838612007-01-30 Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study Tura, Bernardo R Martino, Helena F Gowdak, Luis H dos Santos, Ricardo Ribeiro Dohmann, Hans F Krieger, José E Feitosa, Gilson Vilas-Boas, Fábio Oliveira, Sérgio A Silva, Suzana A Bozza, Augusto Z Borojevic, Radovan de Carvalho, Antonio C Campos Trials Study Protocol BACKGROUND: Cardiovascular diseases are the major cause of death in the world. Current treatments have not been able to reverse this scenario, creating the need for the development of new therapies. Cell therapies have emerged as an alternative for cardiac diseases of distinct causes in experimental animal studies and more recently in clinical trials. METHOD/DESIGN: We have designed clinical trials to test for the efficacy of autologous bone marrow derived mononuclear cell therapies in four different cardiopathies: acute and chronic ischemic heart disease, and Chagasic and dilated cardiomyopathy. All trials are multicenter, randomized, double-blind and placebo controlled. In each trial 300 patients will be enrolled and receive optimized therapy for their specific condition. Additionally, half of the patients will receive the autologous bone marrow cells while the other half will receive placebo (saline with 5% autologous serum). For each trial there are specific inclusion and exclusion criteria and the method for cell delivery is intramyocardial for the chronic ischemic heart disease and intracoronary for all others. Primary endpoint for all studies will be the difference in ejection fraction (determined by Simpson's rule) six and twelve months after intervention in relation to the basal ejection fraction. The main hypothesis of this study is that the patients who receive the autologous bone-marrow stem cell implant will have after a 6 month follow-up a mean increase of 5% in absolute left ventricular ejection fraction in comparison with the control group. DISCUSSION: Many phase I clinical trials using cell therapy for cardiac diseases have already been performed. The few randomized studies have yielded conflicting results, rendering necessary larger well controlled trials to test for efficacy of cell therapies in cardiopathies. The trials registration numbers at the NIH registry are the following: Chagasic cardiomyopathy (NCT00349271), dilated cardiomyopathy (NCT00333827), acute myocardial infarction (NCT00350766) and Chronic Ischemic Heart Disease (NCT00362388). BioMed Central 2007-01-18 /pmc/articles/PMC1783861/ /pubmed/17233910 http://dx.doi.org/10.1186/1745-6215-8-2 Text en Copyright © 2007 Tura et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Tura, Bernardo R
Martino, Helena F
Gowdak, Luis H
dos Santos, Ricardo Ribeiro
Dohmann, Hans F
Krieger, José E
Feitosa, Gilson
Vilas-Boas, Fábio
Oliveira, Sérgio A
Silva, Suzana A
Bozza, Augusto Z
Borojevic, Radovan
de Carvalho, Antonio C Campos
Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study
title Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study
title_full Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study
title_fullStr Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study
title_full_unstemmed Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study
title_short Multicenter randomized trial of cell therapy in cardiopathies – MiHeart Study
title_sort multicenter randomized trial of cell therapy in cardiopathies – miheart study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1783861/
https://www.ncbi.nlm.nih.gov/pubmed/17233910
http://dx.doi.org/10.1186/1745-6215-8-2
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