Umbilical Cord Mesenchymal Stem Cell Improve Cardiac Function on ST-elevation Myocardial Infarction (STEMI) Patients

Sponsor
Indonesia University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05935423
Collaborator
PT. Prodia Stem Cell Indonesia (Industry)
60
1
2
12
5

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to learn about the effectiveness of Umbilical Cord Mesenchymal Stem Cell (UC MSC) therapy in patients with STEMI against infarct myocardial size reduction and prevent the incidence of heart failure in the future

Condition or Disease Intervention/Treatment Phase
  • Biological: Umbilical Cord Mesenchymal Stem Cell transplantation
Phase 3

Detailed Description

Participants who have already done Primary Percutaneous Coronary Intervention (PCI) will be informed about the procedure and risk of this clinical trial. After written consent, 60 participants will be check for their eligibility criteria and randomized into intervention (get UC MSC transplantation) and control group. All participants will be check for their biochemical blood analysis: Interleukin-10 (IL-10), Vascular Endothelial Growth Factor (VEGF), Galectin-3, GATA Binding Protein-4 (GATA-4), and Beclin 1 (1 day before transplantation, 7 dan 14 days after transplantation); infarct size and left ventricular ejection fraction (LVEF) through Cardiac MRI (7-10 days after Primary PCI and 6 months after transplantation) and echocardiography (every month); and major adverse cardiac events/MACE (every month). The result will be access after 6 months follow up.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Intracoronary Allogenic Umbilical Cord Mesenchymal Stem Cell Reduce Infarct Size, Reverse Remodelling, and Improve Cardiac Function
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jul 1, 2024
Anticipated Study Completion Date :
Jul 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: UC-MSC

Patients assigned in UC-MSC intervention group will get Umbilical Cord Mesenchymal Stem Cell transplantation

Biological: Umbilical Cord Mesenchymal Stem Cell transplantation
50 million UC MSC will be transplanted 10-15 days after primary PCI

No Intervention: Control

Patient assigned in control group doesn't get Umbilical Cord Mesenchymal Stem Cell transplantation. However, they will be fully treated based on European Society of Cardiology (ESC) guidelines

Outcome Measures

Primary Outcome Measures

  1. Myocardial infarct size change [6 months]

    Myocardial infarct size change in percentage measure with Cardiac MRI 7-10 days after primary PCI to 6 months after UC-MSC transplantation. The method used by measuring the area of infarction in a series of slices and multiplying the area times the slice thickness to determine a volume.

Secondary Outcome Measures

  1. Left Ventricular Ejection Fraction (LVEF) with Echocardiography [6 months]

    Left Ventricular Ejection Fraction (LVEF) measure with Echocardiography every month within 6 months after UC-MSC transplantation

  2. Left Ventricular Ejection Fraction (LVEF) with Cardiac MRI [6 months]

    Left Ventricular Ejection Fraction (LVEF) measure with Cardiac MRI every month within 6 months after UC-MSC transplantation

  3. Major Cardiac Adverse Event (MACE) [6 months]

    Total death, recurrent myocardial infarction, revascularization with primary PCI or Coronary Artery Bypass Graft (CABG) surgery, stroke, rehospitalisation due to heart failure, haemorrhage and arrythmia malignant assess every months within 6 months after UC-MSC transplantation

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with STEMI treated with primary PCI maximum 12 hours after onset of chest pain
Exclusion Criteria:
  • Patients with history of coronary artery bypass grafting surgery

  • Patients with history of heart failure before admission

  • Patients with cardiogenic shock

  • Patients with cancer disease

  • Patients with malignant arrythmia

  • Patients with chronic kidney disease

  • Patients with haemostasis disorder

  • Patients with infection

  • Patients with stroke

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cipto Mangunkusumo Hospital Jakarta Pusat DKI Jakarta Indonesia

Sponsors and Collaborators

  • Indonesia University
  • PT. Prodia Stem Cell Indonesia

Investigators

  • Principal Investigator: Dede Moeswir, Fakultas Kedokteran Universitas Indonesia

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
dr. Dede Moeswir, Sp.PD, KKV, Principal Investigator, Indonesia University
ClinicalTrials.gov Identifier:
NCT05935423
Other Study ID Numbers:
  • 23-02-0150
First Posted:
Jul 7, 2023
Last Update Posted:
Jul 7, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by dr. Dede Moeswir, Sp.PD, KKV, Principal Investigator, Indonesia University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2023