Randomized Clinical Trial to Evaluate the Regenerative Capacity of CardioCell in Patients With Chronic Ischaemic Heart Failure (CIHF)

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

115

Participants

Timeline

Start Date

April 19, 2018

Primary Completion Date

January 27, 2021

Study Completion Date

March 31, 2021

Conditions
Heart Failure
Interventions
DRUG

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."

DRUG

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.

Trial Locations (5)

04-628

Instytut Kardiologii im. Prymasa Tysiąclecia Stefana Kardynała Wyszyńskiego, Katowice

40-635

Leszek Giec Upper-Silesian Medical Centre of the Silesian Medical University in Katowice, Katowice

31-202

The John Paul II Hospital, Krakow

31-501

The University Hospital in Cracow, Krakow

02-507

Central Clinical Hospital of the MSWiA in Warsaw, Warsaw

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

KCRI

OTHER

collaborator

National Center for Research and Development, Poland

OTHER

lead

John Paul II Hospital, Krakow

OTHER