115
Participants
Start Date
April 19, 2018
Primary Completion Date
January 27, 2021
Study Completion Date
March 31, 2021
CardioCell
"Patients randomized to the active treatment group will receive transcoronary or trans-bypass graft administration of 30 000 000 cells (suspended in 20 ml of 0.9% NaCl and 5% albumin).~Injection will be performed using a dedicated cell delivery catheter. The cell delivery catheter is a typical coronary balloon catheter that is CE marked (1.2x10 mm balloon, RX system) modified to include cell delivery perforations in the balloon section of the catheter. The cell delivery catheter has been demonstrated not to affect cell viability or other cell properties."
Placebos
Patients randomized to the placebo group will receive Placebos consist 0.9% NaCl and 5% albumin injections (in the same volumes as CardioCell) via the coronary arter(ies)/bypass grafts. The CardioCell and placebo are distributed encoded, in an indistinguishable form.
Instytut Kardiologii im. Prymasa Tysiąclecia Stefana Kardynała Wyszyńskiego, Katowice
Leszek Giec Upper-Silesian Medical Centre of the Silesian Medical University in Katowice, Katowice
The John Paul II Hospital, Krakow
The University Hospital in Cracow, Krakow
Central Clinical Hospital of the MSWiA in Warsaw, Warsaw
Collaborators (1)
KCRI
OTHER
National Center for Research and Development, Poland
OTHER
John Paul II Hospital, Krakow
OTHER