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Phase 1 Completed N=21 Randomized Triple-blind Treatment

Intramyocardial Injection of Autologous Aldehyde Dehydrogenase-Bright Stem Cells for Therapeutic Angiogenesis (FOCUS Br)

Source: ClinicalTrials.gov NCT00314366 ↗
Enrolled (actual)
21
Serious AEs
100.0%
Results posted
Nov 2015
Primary outcomePrimary: Safety of Aldehyde Dehydrogenase Bright Stem Cells Versus the Control Group as Measured by Combined Early and Late Adverse Events — 10; 10; 0; 2 participants

Summary

Recent studies have suggested that it may be possible to grow new blood vessels (angiogenesis) to supply the heart muscle that is currently not getting enough blood. One theory is that a certain type of stem cell, aldehyde dehydrogenase bright stem cells, may stimulate the growth of new vessels. After a bone marrow procedure, the special cells are separated and then injected back into the heart around the area of damage with a special guidance and injection system. Once a patient meets all inclusion criteria and no exclusion criteria, he/she will be consented to the study and extensive baseline testing will be completed at St. Luke's Episcopal Hospital in Houston, Texas. Once all baseline criteria are met, the patient has his/her own bone marrow harvested and later injected, if randomized to receive active treatment. The day after the bone marrow harvest, the patient is taken to the cardiac catheterization lab where NOGA mapping is performed and the processed cells or placebo are injected under electromechanical guidance into the affected areas of the left ventricle. The patient is usually discharged home the next day and returns for follow-up at weeks 1 and 4, and months 3 and 6, and at one year unless there is a crossover and then he/she begins baseline again at 6 months and follow-up for one more year. Follow-up testing, including quality of life and NOGA mapping, is done at the time of injection, as well as at 6 months.

Outcome Measures

OutcomeResultp-value
PRIMARY
Safety of Aldehyde Dehydrogenase Bright Stem Cells Versus the Control Group as Measured by Combined Early and Late Adverse Events
10; 10; 0; 2; 2; 0
SECONDARY
New York Heart Association (NYHA) Classification
2.5; 2.6; 2.3; 2.1
SECONDARY
Canadian Cardiovascular (CCS) Angina Score
2.5; 2.5; 2.0; 2.0
SECONDARY
Echocardiography (EF)Percent (%)
36.1; 32.1; 36.0; 34.0
SECONDARY
Left Ventricular End-Systolic Volume (LVESV) (ml)
93.2; 94.9; 85.9; 94.7
SECONDARY
Left Ventricular End-Diastolic Volume (LVEDV)
138.3; 132.7; 127.2; 131.3
SECONDARY
Echocardiography Wall Motion Score Index (WMSI)
1.91; 2.13; 1.90; 2.06
SECONDARY
Myocardial Oxygen Consumption (MVO2)
15.5; 14.1; 17.7; 14.6
SECONDARY
Echocardiography (EF) Percent (%)
38.0; 41.9; 40.4; 42.2
SECONDARY
Total Severity Score (Stress)
798.2; 1007.6; 785.9; 1132
SECONDARY
Total Severity Score (Rest)
542.8; 812.4; 594.6; 828
SECONDARY
Total Severity Score (Reversible)
72.6; 46.5; 22.9; 87.3

Eligibility Criteria

Inclusion Criteria

  • Canadian cardiovascular (CV) Class II-IV angina and/or congestive heart failure (CHF) symptoms
  • Ejection fraction less than or equal to 45%
  • Reversible perfusion defect on single photon emission computed tomography (SPECT)
  • Coronary artery disease (CAD) unable to be corrected by surgery (bypass) or intervention (stent)
  • Able to walk on treadmill
  • Hemodynamically stable

Exclusion Criteria

  • Age less than 18 or greater than 70
  • Atrial fibrillation
  • Severe valve disease
  • History of cancer in last 5 years
  • HIV positive; hepatitis B or C positive.
  • Left ventricular wall thickness less than 8 mm
  • Recent heart attack within the last 30 days
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00314366). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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