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UnknownNCT03351400

Japanese OMI Treatment With Kit-positive Cells for Enhanced Regeneration

Japanese OMI Treatment With Kit-positive Cells for Enhanced Regeneration Trial

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
6 (estimated)
Sponsor
Sakakibara Heart Institute · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the safety and effectiveness of intracoronary infusion of autologous cardiac stem cells in patients with ischemic cardiomyopathy.

Detailed description

This phase I trial will involve 6 patients suffering from chronic ischemic cardiomyopathy and congestive heart failure, to be compared with historical control subjects. This study will be conducted as a collaborative project between the Sakakibara Heart Institute and the CellBank of Japan. The trial is designed to assess the safety and effectiveness of autologous administration of 1,000,000 c-kit-positive cardiac stem cells (CSCs) via intracoronary route following cultivation. The preliminary eligibility criteria will utilize a left ventricular ejection fraction (LVEF) less than 40% measured by echocardiography. During the coronary artery bypass grafting (CABG) surgery, a part (less than 1 gram) of the right atrial appendage (RAA) will be harvested and frozen. When the LVEF is less than 40% after the CABG surgery, the subject will be enrolled as a candidate for the delivery of CSCs, which will be selected from the RAA tissue and cultured for a few months for expansion. The outcome will be evaluated by adverse events as well as cardiac functions.

Conditions

Interventions

TypeNameDescription
BIOLOGICALStem cells administered to participantsPatients in this arm will receive intracoronary infusion of 1,000,000 autologous c-kit positive cardiac stem cells.

Timeline

Start date
2017-11-15
Primary completion
2022-03-01
Completion
2022-03-01
First posted
2017-11-22
Last updated
2021-03-18

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT03351400. Inclusion in this directory is not an endorsement.