search
Back to results

Japanese OMI Treatment With Kit-positive Cells for Enhanced Regeneration (JOKER)

Primary Purpose

Chronic Heart Failure, Old Myocardial Infarction

Status
Unknown status
Phase
Phase 1
Locations
Japan
Study Type
Interventional
Intervention
Stem cells administered to participants
Sponsored by
Sakakibara Heart Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Heart Failure focused on measuring cardiac stem cells, c-kit

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult with ability to provide informed consent.
  • Left ventricular ejection fraction less than 40% as evidenced by echocardiogram.
  • Scheduled for elective surgical revascularization within 2 months.

Exclusion Criteria:

  • Positive for HBs-Ag, HCV-Ab, HIV-Ab, or tests for syphilis.
  • Diabetic HbA1c greater than 8.5%.
  • Pregnant women.
  • Scheduled for additional interventions including ventriculoplasty.

Sites / Locations

  • Sakakibara Heart Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment group

Arm Description

Stem cells administered to participants

Outcomes

Primary Outcome Measures

Monitoring adverse events
Including death, ventricular arrhythmia, bleeding, myocardial infarction, cardiac tumor, brain stroke, peripheral embolism

Secondary Outcome Measures

NYHA classification
Measurement of symptom
Serum NT-proBNP
Measurement of cardiac function
Electrocardiogram
Measurement of arrhythmia
Chest X-ray
Measurement of cardiac function
Cardiopulmonary exercise test
Measurement of cardiopulmonary function
Echocardiogram
Measurement of cardiac function
Magnetic resonance imaging
Measurement of cardiac function
Myocardial scintigraphy
Measurement of myocardial viability

Full Information

First Posted
November 14, 2017
Last Updated
March 17, 2021
Sponsor
Sakakibara Heart Institute
Collaborators
CellBank of Japan
search

1. Study Identification

Unique Protocol Identification Number
NCT03351400
Brief Title
Japanese OMI Treatment With Kit-positive Cells for Enhanced Regeneration
Acronym
JOKER
Official Title
Japanese OMI Treatment With Kit-positive Cells for Enhanced Regeneration Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 15, 2017 (Actual)
Primary Completion Date
March 2022 (Anticipated)
Study Completion Date
March 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sakakibara Heart Institute
Collaborators
CellBank of Japan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Heart Failure, Old Myocardial Infarction
Keywords
cardiac stem cells, c-kit

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
6 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment group
Arm Type
Experimental
Arm Description
Stem cells administered to participants
Intervention Type
Biological
Intervention Name(s)
Stem cells administered to participants
Intervention Description
Patients in this arm will receive intracoronary infusion of 1,000,000 autologous c-kit positive cardiac stem cells.
Primary Outcome Measure Information:
Title
Monitoring adverse events
Description
Including death, ventricular arrhythmia, bleeding, myocardial infarction, cardiac tumor, brain stroke, peripheral embolism
Time Frame
2 years
Secondary Outcome Measure Information:
Title
NYHA classification
Description
Measurement of symptom
Time Frame
2 years
Title
Serum NT-proBNP
Description
Measurement of cardiac function
Time Frame
2 years
Title
Electrocardiogram
Description
Measurement of arrhythmia
Time Frame
2 years
Title
Chest X-ray
Description
Measurement of cardiac function
Time Frame
2 years
Title
Cardiopulmonary exercise test
Description
Measurement of cardiopulmonary function
Time Frame
2 years
Title
Echocardiogram
Description
Measurement of cardiac function
Time Frame
2 years
Title
Magnetic resonance imaging
Description
Measurement of cardiac function
Time Frame
2 years
Title
Myocardial scintigraphy
Description
Measurement of myocardial viability
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult with ability to provide informed consent. Left ventricular ejection fraction less than 40% as evidenced by echocardiogram. Scheduled for elective surgical revascularization within 2 months. Exclusion Criteria: Positive for HBs-Ag, HCV-Ab, HIV-Ab, or tests for syphilis. Diabetic HbA1c greater than 8.5%. Pregnant women. Scheduled for additional interventions including ventriculoplasty.
Facility Information:
Facility Name
Sakakibara Heart Institute
City
Tokyo
ZIP/Postal Code
183-0003
Country
Japan

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
22965994
Citation
Chugh AR, Beache GM, Loughran JH, Mewton N, Elmore JB, Kajstura J, Pappas P, Tatooles A, Stoddard MF, Lima JA, Slaughter MS, Anversa P, Bolli R. Administration of cardiac stem cells in patients with ischemic cardiomyopathy: the SCIPIO trial: surgical aspects and interim analysis of myocardial function and viability by magnetic resonance. Circulation. 2012 Sep 11;126(11 Suppl 1):S54-64. doi: 10.1161/CIRCULATIONAHA.112.092627.
Results Reference
background

Learn more about this trial

Japanese OMI Treatment With Kit-positive Cells for Enhanced Regeneration

We'll reach out to this number within 24 hrs