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Intracoronary Autologous Stem Cell Transplantation in ST Elevation Myocardial Infarction: TRACIA STUDY.

Intracoronary Autologous Stem Cell Transplantation in ST Elevation Myocardial Infarction: TRACIA Study.

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00725738
Acronym
TRACIA
Enrollment
80
Registered
2008-07-30
Start date
2008-05-31
Completion date
2009-12-31
Last updated
2008-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction

Keywords

Myocardial, Infarction,, Stem, Cell, Therapy

Brief summary

The purpose of this study is to evaluate the ejection fraction (EF) increase at 6 months follow up and major adverse cardiovascular events (MACE) after intracoronary autologous stem cell transplantation in ST elevation myocardial infarction patients versus a control group.

Detailed description

Experimental trials with bone marrow cell have suggested that adult stem cell can contribute to regeneration of infarcted myocardial muscle and increase the neovascularization of the ischemic tissue. Post-myocardial infarction heart failure secondary to ventricular remodelation it's an increasing problem. A novel therapeutic approach for decrease this consequence is to induce the angiogeneses and regeneration of myocardial cells. Many trials have shown benefits through the intracoronary injection of stem cell, however the clinical benefit is still controversial. The present trial is a randomized single blinded controlled trial designed to evaluate the improvement on EF and survival in post ST elevation myocardial infarction patients undergoing to intracoronary autologous stem cell transplantation.

Interventions

GENETICStem Cell Transplantation

1-2 million of CD34 cells injected through the infarct related artery by PTCA over-the-wire catheter during multiple sequences of balloon artery occlusion with a mean duration of 30 minutes.

Sponsors

National Center of Blood Transfusion Mexico.
CollaboratorUNKNOWN
National Heart Institute, Mexico
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Both gender patients between 20 and 75 years old with an acute myocardial infarction (less 24 hrs of symptoms) undergoing to primary angioplasty. * LVEF \< o = 45% by MRI, radioisotopic ventriculography or echocardiogram. * Informed written consent.

Exclusion criteria

* Cardiogenic Shock. * Post-myocardial infarction mechanical complication * Malignant ventricular arrythmias * History of malignant disease during the last five years. * Pregnancy * Renal chronic disease with a creatinine level \> 2.6 mg/dl. * Any kind of stroke during the last year. * Any chronic disease that can affect the patient survival during the trial.

Design outcomes

Primary

MeasureTime frame
Evaluate the mean LVEF increase by magnetic resonance imaging (MRI) at 6 months of follow up between the stem cell group and the control group.6 months

Secondary

MeasureTime frame
Evaluate the left ventricular end diastolic volume (LVEDV) and left ventricular end systolic volume (LVESV)with image magnetic resonance(IMR) at 6 months follow up between stem cell and control group.6 months
Evaluate the oxygen consumption during treadmill stress test (MVO2) by expired gases analysis and the incidence of MACE at 6 months follow up between stem cell and control group.6 months

Countries

Mexico

Contacts

Primary ContactMarco A Peña-Duque, MD
penmar@cardiologia.org.mx55732911
Backup ContactLuis J Uribe-González, MD, MSc
ljhonathanug@hotmail.com55732911

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026