Key result
This study protocol outlines a planned phase IIb trial to evaluate whether intracoronary injection of autologous bone marrow mononuclear cells improves left ventricular ejection fraction in patients with idiopathic dilated cardiomyopathy.
Why the study?
Intracoronary BMMNC infusion improves ventricular function after acute myocardial infarction, but less information is available about its role in non-ischemic dilated myocardiopathies.
Does a single dose of intracoronary autologous bone marrow mononuclear cells improve left ventricular ejection fraction in patients with idiopathic dilated cardiomyopathy?
RCT (n=51)
Double-blind
2:1 block randomization
Yes
Does a single dose of intracoronary autologous bone marrow mononuclear cells improve left ventricular ejection fraction in patients with idiopathic dilated cardiomyopathy?
Answers are grounded in this paper and cite their sources.
This study protocol describes a randomized controlled trial to evaluate the efficacy of intracoronary autologous bone marrow mononuclear cells for improving ventricular function in non-ischemic dilated cardiomyopathy.
BACKGROUND: Cellular therapies have been increasingly applied to diverse human diseases. Intracoronary infusion of bone marrow-derived mononuclear cells (BMMNC) has demonstrated to improve ventricular function after acute myocardial infarction. However, less information is available about the role of BMMNC therapy for the treatment of dilated myocardiopathies (DCs) of non-ischemic origin. This article presents the methodological description of a study aimed at investigating the efficacy of intracoronary injection of autologous BMMNCs in the improvement of the ventricular function of patients with DC. METHODS: This randomised, placebo-controlled, double-blinded phase IIb clinical trial compares the improvement on ventricular function (measured by the changes on the ejection fraction) of patients receiving the conventional treatment for DC in combination with a single dose of an intracoronary infusion of BMMNCs, with the functional recovery of patients receiving placebo plus conventional treatment. Patients assigned to both treatment groups are monitored for 24 months. This clinical trial is powered enough to detect a change in Left Ventricular Ejection Fraction (LVEF) equal to or greater than 9%, although an interim analysis is planned to re-calculate sample size. DISCUSSION: The study protocol was approved by the Andalusian Coordinating Ethics Committee for Biomedical Research (Comité Coordinador de Ética en Investigación Biomédica de Andalucia), the Spanish Medicines and Medical Devices Agency (Agencia Española de Medicamentos y Productos Sanitarios), and is registered at the EU Clinical Trials Register (EudraCT: 2013-002015-98). The publication of the trial results in scientific journals will be performed in accordance with the applicable regulations and guidelines to clinical trials. TRIAL REGISTRATION: ClinicalTrials.gov Identifier NCT02033278 (First Posted January 10, 2014): https://clinicaltrials.gov/ct2/show/NCT02033278 ; EudraCT number: 2013-002015-98, EU CT Register: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2013-002015-98 . Trial results will also be published according to the CONSORT statement at conferences and reported peer-reviewed journals.
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Romero et al. (2019) conducted an RCT in Idiopathic dilated cardiomyopathy (n=51). Autologous bone marrow mononuclear cells (BMMNCs) vs. Placebo was evaluated on Angiographic changes in global LVEF at 6 months after cell infusion. This study protocol outlines a planned phase IIb trial to evaluate whether intracoronary injection of autologous bone marrow mononuclear cells improves left ventricular ejection fraction in patients with idiopathic dilated cardiomyopathy.
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