University of Kentucky Healthcare
Lexington, Kentucky, 40536, United States
NCT Number: NCT03043742
Assess the safety and effectiveness of stem cell application with regard to improvement in regional myocardial function in patients receiving Trans-Myocardial Laser Revascularization (TMR) and stem cells.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
Lexington, Kentucky, 40536, United States
Multiple case experiences and studies have been published reviewing clinical experiences with Carbon Dioxide Trans-Myocardial Laser Revascularization (TMR) and autologous bone marrow derived cell application. These experiences have demonstrated perfusion improvements, ejection fraction improvements and improvements in angina or heart failure symptoms. The investigators elected to examine the use of CD133 positive (CD133+) BM-derived stem cells because of their pluripotent nature and the fact that during the CD133 selection process inflammatory cells present in the bone marrow are being discarded. CD133+ is a recently discovered marker for more primitive bone marrow derived multipotent stem and endothelial progenitor cells and is of particular interest in studies directed to therapeutic angiogenesis, as these cells have been shown to differentiate into endothelial and myogenic cell lines. Multiple studies have utilized BM derived cells for myocardial regeneration. Patients who received CD133+ cells showed improved perfusion at injection sites of stem cells leading to a significant increase in volume of left ventricular ejection fraction, regional wall motion in the infarct zone, and a reduction in end systolic left ventricular volume.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Injection of bone marrow derived autologous CD133+ cell product into laser channels during Trans-Myocardial Revascularization
Other names: Stem cell
Time frame: Assess from Procedure through 12 months
Major adverse cardiac event and adverse events defined in the common toxicity criteria
Time frame: Assessed at baseline, 6 months, and 12 months
Measured as a percentage by Echocardiography
Time frame: Assessed at baseline and 6 months
Measured by nuclear scanning.
Time frame: Assessed at baseline and 6 months
Measured by nuclear scanning.
Time frame: Assessed at baseline, 3 months, 6 months, and 12 months
Measured in feet during a 6 minute walk test
Time frame: Assessed at baseline, 3 months, 6 months, and 12 months
Measured using the Kansas City Cardiomyopathy Questionnaire.
Time frame: Assessed at baseline, 3 months, 6 months, and 12 months.
Measured using the Canadian Cardiovascular Society Grading Scale.
Time frame: Assessed at baseline, 3 months, 6 months, and 12 months.
Measured using the New York Heart Association Questionnaire
Time frame: Assessed at baseline, 6 months, and 12 months
Measured using echocardiogram.
Time frame: Assessed at baseline, 3 months, 6 months, and 12 months
Measured using the Seattle Angina Questionnaire
Michael Sekela
Other
Prospective Controlled Trial of Intra-Myocardial Infusion of Bone Marrow Derived Autologous CD133+ Selected Cells During Trans-Myocardial Laser Revascularization (TMR) in Patients With Chronic Ischemic Heart Disease
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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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