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Not yet recruiting NCT04052191

MCRcI® Stem Cell Treatment for Diffuse Coronary Artery Disease

Phase I Interventional Coronary Artery Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: MCRcI® stem cells.
Who it may be relevant to
Registry conditions: Coronary Artery Disease. Basic parameters: 20 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Intra-Coronary Administration of MCRcI® (Myo-Cardial Regenerative Cellular Injection) Improves Left Ventricular Function in Patients With Diffuse Coronary Artery Disease

Overview

Safety evaluation of Intra-Coronary Administration of MCRcI® stem cells in Patients with Diffuse Coronary Artery Disease.

Interventions

  • Biological MCRcI® stem cells
    Intra-Coronary Administration of MCRcI® stem cells

Primary outcome measures

  • Incidence of Treatment Emergent Adverse Events [Time frame: 6 months]
Secondary outcome measures (4)
  • Left ventricle stroke volume [Time frame: 12 months]
  • End diastolic volume [Time frame: 12 months]
  • Left ventricular ejection fraction (LVEF) [Time frame: 12 months]
  • Severity of angina symptom using Canadian Cardiovascular Society grading. [Time frame: 12 months]

Eligibility criteria

Inclusion criteria

  • Patients with Diffuse Coronary Artery Disease
  • Age 20\~80
  • Participants have received proper medication
  • Canadian Cardiovascular Society class II- IV Angina.

Exclusion criteria

  • Age <20 or >80
  • Pregnant or breast feeding
  • Positive adventitious infection (such as HIV, hepatitis )
  • History of Myocardial Infarction within past 3 months
  • Severe aortic or mitral valve narrowing
  • Short of breath unable to receive PCI examination or treatment
  • Malignant tumor
  • Hematopoietic dysplasia
  • Severe organ disease with less than 1 year of life expectancy
  • Chronic kidney disease with CCr<20ml/min
  • Kiney disease on renal dialysis.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Sequential
Masking
Single blind
Primary purpose
Treatment

Study locations

Taiwan · 1 center
  • HONYA Medical Inc — Tainan

Identifiers

NCT: NCT04052191 · KCG17121910001

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗