INCL - National Institute of Cardiology Laranjeiras
Rio de Janeiro, 22.240-006, Brazil
NCT Number: NCT00333827
The purpose of this study is to determine effect of cell therapy in patients with severe dilated cardiomyopathy
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Notify Me18 year–65 year
All sexes
Interventional
Phase 3
Rio de Janeiro, 22.240-006, Brazil
This protocol describes a double-blind placebo controlled randomized clinical trial to evaluate the efficacy of bone marrow derived stem cell implants in 300 bazillion patients with dilated cardiomyopathy and heart failure in class III or IV of the New York Heart Association.
The primary endpoint of this study is to evaluate the effect of the autologous bone marrow stem cell implant in the increase of the ejection fraction of the left ventricle in comparison with a control group, under optimized therapy for dilated cardiomyopathy. Secondary endpoints will evaluate the alteration in NYHA functional class, mortality rate, physical capacity (by ergoespirometry), life quality (Minnesota questionnaire) and pulmonary congestion in dilated cardiomyopathy patients the received the autologous bone-marrow stem cell implant.
Hypothesis: The main hypothesis of this study is that the patients who received the autologous bone-marrow stem cell implant will have after a 6 month follow-up a mean 5% increase in absolute left ventricle ejection fraction in comparison with the control group.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
optimal therapy for cardiaca failure
stem cell
Time frame: 6 months
Time frame: 1 year
Time frame: 1 year
Time frame: 6 month
Time frame: 6 month
Time frame: 1 year
Ministry of Health, Brazil
Other Gov
Multicenter Randomized Study Of Cell Therapy In Cardiopathies - Dilated Cardiomyopathy
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