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Transepicardial With Transseptal Autologous CD 133+ Bone Marrow Cell Implantation in Patient Following CABG Surgery

Primary Purpose

Coronary Artery Disease

Status
Completed
Phase
Phase 4
Locations
Indonesia
Study Type
Interventional
Intervention
Transepicardial with Transseptal CD 133+ Implantation
Sponsored by
National Cardiovascular Center Harapan Kita Hospital Indonesia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring CD 133+, Transepicardial with Transseptal Implantation, CABG

Eligibility Criteria

40 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with coronary artery disease 3 vessels disease indicated for CABG
  • LVEF < 35% which has been confirmed by MRI
  • Patients with akinetic or hypokineic segment, and left ventricle myocardial hypoperfusion confirmed in MRI
  • has signed informed consent

Exclusion Criteria:

Emergency CABG Ungraftable coronary artery Acute myocardial Infarct (<14 days) Valve disease which need surgery repair Contraindicated for MRI High degree ventricular arrhytmia Coagulation disorder HIV positive patient, Hepatitis B + patients, HCV + patients AST/ALT > 1,5 upper normal value Creatinine > 2 g/dl. Malignancy

Drop out criteria :

Aortic cross clamp >120 minutes and CABG total time >180

Sites / Locations

  • National Cardiovascular Center Harapan Kita

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

subject

control

Arm Description

this arm will receive Transepicardial with Transseptal CD 133+ Implantation

this arm will not receive Transepicardial with Transseptal CD 133+ Implantation

Outcomes

Primary Outcome Measures

Myocardial Defect Perfusion
Number of heart wall segments with perfusion defect measured by MRI.
Left Ventricular Ejection Fraction
Left ventricular ejection fraction (LVEF) measured by MRI. Normal range of LVEF ranges from 50% to 70%. Borderline LVEF ranges from 41% to 49% Reduced LVEF ranges < 41%

Secondary Outcome Measures

Six Minutes Walking Test
Quality of life will be assessed using Six minutes walking test, to see the changes of six minutes walking test before and after intervention Distances reported for healthy individuals ages 40 yo 85 years range from 400 to 700 m..
Wall Motion Score Index
Cardiac wall motion abnormality will be measured using Wall Motion Score Index with MRI. Each myocardial segment is assigned a score from 1 to 4. The 16 segment model of myocardial segmentation is recommended. A WMSI of 1.0 is considered normokinetic. A WMSI of 1.5 is considered mild hypokinesia A WMSI of 2.0 is considered hypokinesia A WMSI of 2.5 is considered severe hypokinesia A WMSI of 3.0 is considered akinetic.
Myocardial Scar Size
Percentage of myocardial scar size proportion measured by MRI to quantify and define the extent/transmurality of scar tissue, the following definitions were used spatial (circumferential) extent, the number of affected segments nontransmurality, the number of segmments with a segmental scar score of 1 or 2, and transmurality, the number of segments with a segmental scar score of 3 or 4 total score, summed segmental scar scores per patient divided by 17 (which reflects the damage per patient)
Vascular Endothelial Growth Factor
Cytokine that has important role for angiogenesis. Normal range for plasma VEGF is 0-115 pg/ml
Left Ventricle End Systolic Volume
Left ventricle end-systolic volume is the volume of blood in a left ventricle at the end of contraction, or systole, and the beginning of filling, or diastole. Normal LVESV ranges is 37 - 57 mililiters.
Minnesota Living With Heart Failure Questionnaire
Quality of life assessed using Minnesota Living With Heart Failure Questionnaire consist of 21 questions, to see the changes before and after intervention. Minimum score = 0, Maximum score = 105 Higher values represent a worse outcome
Left Ventricle End Diastolic Volume
Left ventricle end-diastolic volume is the volume of blood in the left ventricle at end load or filling in (diastole) or the amount of blood in the ventricle just before systole. Normal ranges of LVEDV is 121 - 163 mililiters

Full Information

First Posted
August 7, 2016
Last Updated
March 16, 2020
Sponsor
National Cardiovascular Center Harapan Kita Hospital Indonesia
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1. Study Identification

Unique Protocol Identification Number
NCT02870933
Brief Title
Transepicardial With Transseptal Autologous CD 133+ Bone Marrow Cell Implantation in Patient Following CABG Surgery
Official Title
The Effect of Transepicardial Augmentation on Transseptal Autologous CD 133+ Bone Marrow Cell Implantation to Myocardial Perfusion in Patient Following Coronary Artery Bypass Grafting
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
January 2016 (undefined)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
April 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Cardiovascular Center Harapan Kita Hospital Indonesia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Heart Failure has several etiologies and one of them is coronary artery disease. Coronary artery bypass grafting (CABG) is one of revascularizations method which has been used for decades in coronary artery disease theraphy. However, data about coronary artery bypass grafting shows that post-CABG patients still have low ejection fraction. For the last decade, there have been a lot of studies about the using of stem cells to increase heart contractility and reverse the heart remodelling process. In this study, we use CD 133+ bone marrow stem cells which has been proved to have higher angiogenesis potential. The stem cells is given during CABG by injection transepicardial and transseptal. The purpose of this study is to determine whether transpicardial and transseptal injection of CD 133+ bone marrow stem cells can improve myocardial perfusion in patient with low ejection fraction following CABG surgery.
Detailed Description
Study sample : patient with low ejection fraction indicated for CABG surgery in NCCHK who fulfill inclusion and exclusion criteria Sampling method : first we use consecutive method to find subject with male sex and age 40-70. After that, we use simple random sampling to allocate each subject to each group. Total samples is 13 for each group. To anticipated drop out rate 10%, total sample is 15 for each group. Intervention and measurement : Control group will only receive CABG surgery. Study group will receive CBAG surgery and stem cell implantation. Stem cell aspiration will be performed 1 day before CABG procedure. Before aspiration, patients will be given local anesthetic and light sedation. Stem cell will be collected from posterior iliac crest. Total aspirate 190 cc. Stem cell CD133+ will be separated using CliniMACS® Magnetic Separation Device after labelled with Magnetic microbeads - anti CD133 labelling. Myocardial perfusion reserve index will be measure using MRI. MPRI value will be obtained globally and segmentally in each 16 ventricle segments VEGF plasma level will be measured using sandwich Enzyme-linked Immunosorbent Assay method. Ejection fraction, left ventricle dimension, and scar size will be measured using MRI. Quality of life will be measured using Minnesota Living With Heart Failure Questionnaire. Statistical analysis is done using IBM SPSS Statistics version 21.0 (SPSS inc, Chicago, IL, USA). Numerical data will be presented in either mean/standard deviation or median/min-max depend on distribution of data. Hypothesis test for numeric variable is done using paired/non-paired T test or Mann-Whitney/Wilcoxon depend on normality of data. Normality test is done using Shapiro-Wilk test. Hypothesis test for category varible is done using chi-square or fischer test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
CD 133+, Transepicardial with Transseptal Implantation, CABG

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
subject
Arm Type
Experimental
Arm Description
this arm will receive Transepicardial with Transseptal CD 133+ Implantation
Arm Title
control
Arm Type
No Intervention
Arm Description
this arm will not receive Transepicardial with Transseptal CD 133+ Implantation
Intervention Type
Biological
Intervention Name(s)
Transepicardial with Transseptal CD 133+ Implantation
Intervention Description
Transepicardial with Transseptal CD 133+ Implantation
Primary Outcome Measure Information:
Title
Myocardial Defect Perfusion
Description
Number of heart wall segments with perfusion defect measured by MRI.
Time Frame
Baseline, 6 months
Title
Left Ventricular Ejection Fraction
Description
Left ventricular ejection fraction (LVEF) measured by MRI. Normal range of LVEF ranges from 50% to 70%. Borderline LVEF ranges from 41% to 49% Reduced LVEF ranges < 41%
Time Frame
Baseline, 6 months
Secondary Outcome Measure Information:
Title
Six Minutes Walking Test
Description
Quality of life will be assessed using Six minutes walking test, to see the changes of six minutes walking test before and after intervention Distances reported for healthy individuals ages 40 yo 85 years range from 400 to 700 m..
Time Frame
Baseline, 6 months
Title
Wall Motion Score Index
Description
Cardiac wall motion abnormality will be measured using Wall Motion Score Index with MRI. Each myocardial segment is assigned a score from 1 to 4. The 16 segment model of myocardial segmentation is recommended. A WMSI of 1.0 is considered normokinetic. A WMSI of 1.5 is considered mild hypokinesia A WMSI of 2.0 is considered hypokinesia A WMSI of 2.5 is considered severe hypokinesia A WMSI of 3.0 is considered akinetic.
Time Frame
Baseline, 6 months
Title
Myocardial Scar Size
Description
Percentage of myocardial scar size proportion measured by MRI to quantify and define the extent/transmurality of scar tissue, the following definitions were used spatial (circumferential) extent, the number of affected segments nontransmurality, the number of segmments with a segmental scar score of 1 or 2, and transmurality, the number of segments with a segmental scar score of 3 or 4 total score, summed segmental scar scores per patient divided by 17 (which reflects the damage per patient)
Time Frame
Baseline, 6 months
Title
Vascular Endothelial Growth Factor
Description
Cytokine that has important role for angiogenesis. Normal range for plasma VEGF is 0-115 pg/ml
Time Frame
Baseline, 6 months
Title
Left Ventricle End Systolic Volume
Description
Left ventricle end-systolic volume is the volume of blood in a left ventricle at the end of contraction, or systole, and the beginning of filling, or diastole. Normal LVESV ranges is 37 - 57 mililiters.
Time Frame
Baseline, 6 months
Title
Minnesota Living With Heart Failure Questionnaire
Description
Quality of life assessed using Minnesota Living With Heart Failure Questionnaire consist of 21 questions, to see the changes before and after intervention. Minimum score = 0, Maximum score = 105 Higher values represent a worse outcome
Time Frame
Baseline, 6 months
Title
Left Ventricle End Diastolic Volume
Description
Left ventricle end-diastolic volume is the volume of blood in the left ventricle at end load or filling in (diastole) or the amount of blood in the ventricle just before systole. Normal ranges of LVEDV is 121 - 163 mililiters
Time Frame
Baseline, 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with coronary artery disease 3 vessels disease indicated for CABG LVEF < 35% which has been confirmed by MRI Patients with akinetic or hypokineic segment, and left ventricle myocardial hypoperfusion confirmed in MRI has signed informed consent Exclusion Criteria: Emergency CABG Ungraftable coronary artery Acute myocardial Infarct (<14 days) Valve disease which need surgery repair Contraindicated for MRI High degree ventricular arrhytmia Coagulation disorder HIV positive patient, Hepatitis B + patients, HCV + patients AST/ALT > 1,5 upper normal value Creatinine > 2 g/dl. Malignancy Drop out criteria : Aortic cross clamp >120 minutes and CABG total time >180
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tri Wisesa Soetisna, MD, MHA
Organizational Affiliation
National Cardiovascular Center Harapan Kita
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Cardiovascular Center Harapan Kita
City
Jakarta
State/Province
DKI Jakarta
ZIP/Postal Code
11420
Country
Indonesia

12. IPD Sharing Statement

Plan to Share IPD
Yes

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Transepicardial With Transseptal Autologous CD 133+ Bone Marrow Cell Implantation in Patient Following CABG Surgery

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