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Completed

NCT Number: NCT00333827

Cell Therapy In Dilated Cardiomyopathy

The purpose of this study is to determine effect of cell therapy in patients with severe dilated cardiomyopathy

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

INCL - National Institute of Cardiology Laranjeiras

Rio de Janeiro, 22.240-006, Brazil

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of dilated cardiomyopathy according to WHO criteria
  • Syndromic heart failure in functional class III or IV of the NYHA
  • Enrollment and continuous follow-up in cardiac out-patient clinic
  • Adequate medical therapy after optimization therapy
  • Echocardiogram with an ejection fraction equal to or less than 35% by Simpson's rule

Exclusion criteria

  • Valvular diseases, except functional mitral or tricuspid reflow
  • Coronariography showing a significant lesion (obstruction of at least 50% of the lumen in the troncus or the main arteries - LAD, CX, RC) in one or more arteries
  • Serologic diagnosis for Chagas disease or at least two of the following criteria: epidemiology, right bundle branch block, anterior hemi-block, apical aneurism
  • Sustained ventricular tachycardia
  • Abusive use of alcohol or illicit drugs
  • Pregnancy
  • Use of cardio toxic drugs
  • Any co-morbidity with impact in life expectancy in 2 years
  • Renal function compromised (creatinine above 2 mg/dl)

Treatment and study plan

optimal therapy for cardiaca failure

Drug

optimal therapy for cardiaca failure

cell

Procedure

stem cell

Primary outcomes

  1. increase of the ejection fraction of the left ventricle

    Time frame: 6 months

Secondary outcomes

  1. Death by any cause

    Time frame: 1 year

  2. Maximum oxygen consumption difference, as measured by ergoespirometry, at six and twelve months in relation to baseline

    Time frame: 1 year

  3. Difference in life quality as estimated by Minnesota living with Heart Failure Questionnaire

    Time frame: 6 month

  4. Difference in NYHA functional class

    Time frame: 6 month

  5. Percent number of patients that reached an absolute increase of 5% in ejection fraction

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Ministry of Health, Brazil

Other Gov

Collaborators

  • Financiadora de Estudos e Projetos

Registry information

Official study title

Multicenter Randomized Study Of Cell Therapy In Cardiopathies - Dilated Cardiomyopathy

Important dates

Study start
2006
Primary completion
2012
Study completion
2013
First posted
Jun 6, 2006
Registry last updated
Mar 13, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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