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Clinical Use of Stem Cells for the Treatment of Covid-19

Primary Purpose

Covid19, Pneumonia, Multiple Organ Failure

Status
Completed
Phase
Phase 1
Locations
Turkey
Study Type
Interventional
Intervention
MSC Treatment
Saline Control
Sponsored by
SBÜ Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring Covid-19, Pneumonia, Multiple Organ Failure, Coronavirus, Mesenchymal stem cells, Cellular therapy

Eligibility Criteria

40 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 40-60 years old male or female
  • Confirmed 2019-nCoV infection with RT-PCR Laboratory test
  • Confirmed Pneumonia with chest radiography and computer tomography
  • and any of the following criteria:

    1. Shortness of breath (RR ≥30/min)
    2. Resting finger oxygen saturation 93%
    3. Arterial oxygen partial pressure (PaO2)/oxygen absorption concentration (FiO2) ≤ 300MMHG
    4. Advancing of focus in Pulmonary imaging to >50% in 24-48 hours

Exclusion Criteria:

  • Those who are not pregnant, breastfeeding and pregnant but who do not take effective contraceptive measures;
  • Patients with malignant tumors, other serious systemic diseases and psychosis;
  • Informed consent is not given or does not comply with the test requirements.
  • Co-infection of HIV, tuberculosis, influenza virus, adenovirus and other respiratory infection virus.
  • Pneumonia caused by bacteria, mycoplasma, chlamydia, legionella, fungi or co-infection of HIV, tuberculosis, influenza virus, adenovirus and other respiratory infection virus.
  • Obstructive HABP / VABP caused by lung cancer or other known causes; Long-term history of use of immunosuppressive agents;
  • History of epilepsy and need for continuous anticonvulsant therapy or anticonvulsant therapy taken within 3 years;
  • Invasive ventilation
  • Shock
  • Other organ failures

Sites / Locations

  • Istinye University
  • SBÜ Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Sham Comparator

Experimental

Arm Label

Untreated

Saline Control

Experimental UC-MSCs

Arm Description

Group 1: patients that are not on a ventilator (n=10) No extra intervention will be done.

Group 2: patients that are on a ventilator and will receive saline injections (n=10) as control for MSC transplantation group (3).

Group 3: patients that are on a ventilator and will receive MSC transplantation injections (n=10)

Outcomes

Primary Outcome Measures

Clinical improvement
Improvement of clinical symptoms related to Covid-19 infection (fever, pneumonia, shortness of breath)

Secondary Outcome Measures

Lung damage improvement
Improvement of lungs assessed by CT Scan
Sars-Cov-2 viral infection laboratory test
Negative, measured by RT-PCR laboratory tests for the virus
Blood test
Cell types and numbers

Full Information

First Posted
April 25, 2020
Last Updated
May 22, 2021
Sponsor
SBÜ Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi
Collaborators
Istinye University, Regenerative Medicine and Stem Cell Production Center Liv MedCell, Liv Hospital (Ulus)
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1. Study Identification

Unique Protocol Identification Number
NCT04392778
Brief Title
Clinical Use of Stem Cells for the Treatment of Covid-19
Official Title
What is the Effect of Mesenchymal Stem Cell Therapy on Seriously Ill Patients With Covid 19 in Intensive Care? (Prospective Double Controlled Study)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
April 1, 2020 (Actual)
Primary Completion Date
November 1, 2020 (Actual)
Study Completion Date
November 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
SBÜ Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi
Collaborators
Istinye University, Regenerative Medicine and Stem Cell Production Center Liv MedCell, Liv Hospital (Ulus)

4. Oversight

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

5. Study Description

Brief Summary
This study aims to use the regenerative and repair abilities of stem cells to fight against the harmful effects of the novel coronavirus Covid-19 and therefore develop a treatment strategy. It is known that fatalities from this virus is largely caused by its damage to lungs and other organs. As the disease progresses, these organs fail and lead to mortality. Our hope is that the stem cell transplantation from healthy donors will repair the damage caused by the virus and result in a healthy recovery.
Detailed Description
Introduction: The COVID-19 corona virus epidemic has spread from Wuhan, China to the whole world, and has been declared a pandemic by WHO worldwide. In severe patients, ARDS and multiple organ failure can be seen. This condition is associated with cytokine storm in the body. When the virus invades the body, dentric cells can activate macrophages, lymphocytes and natural killer cells. Mesenchymal stem cells (MKH) not only inhibit the abnormal activation of T lymphocytes and macrophages, but also encourage them to differentiate into regulatory T cell subsets (Treg) clusters and anti-inflammatory macrophages. MSCs application proved therapeutic efficiency during influenza infection resulting in reduced impairment of alveolar fluid clearance and lung injury. This was attributed towards attenuation of pro-inflammatory cytokine secretion, inflammatory cell recruitment and increased alveolar macrophages content. Aim of study: To provide immune modulation to patients with COVID-19 who are taken to intensive care and resistant to treatment by performing MSCs transplantation and to reduce the damage caused by cytokin storm to tissues and organs, Correcting immunosuppression in patients and increasing the fight against COVID-19 virus by CD4+T, CD+8T cellular cell arrangement, It is to accelerate the recovery in organ damage by increasing growth factors by means of MSCs. Materials and method: Patients diagnosed with COVID-19 infection as clinically, radiologically and laboratory-wise will be divided into three groups: Group 1: patients that are not on a ventilator (n=10) Group 2: patients that are on a ventilator and will receive saline injections (n=10) Group 3: patients that are on a ventilator and will receive MSC transplantation injections (n=10) Mesenchymal stem cells originating from allogenic umbilical cord produced under GMP conditions will be administered in 3 times, with doses indicated below, intravenously within 1 week. Dose: Application: 3 million cells / kg IV ---------------------------------------- --------- 1 day Application: 3 million cells / kg IV ---------------------------------------- --------- 3. Day Application: 3 million cells / kg IV ---------------------------------------- --------- 6. Day The blood will be analyzed for the expression levels of growth factors, including vascular endothelial growth factor, fibroblast growth factor, platelet derived-growth factor, epidermal growth factor, transforming growth factor beta, hepatocyte growth factor, nerve growth factor, VEGF receptor (VEGFR), angiopoietin1 (Angpt-1), and Angpt-2, using sandwich enzyme-linked immune sorbent assays (ELISAs). Investigators also analyzed the caspase-3 system in the blood. immunoassay kits will be used for analyses in accordance with the manufacturer's instructions. Biochemical parameters of the liver, such as alanine transaminase (ALT), aspartate transaminase (AST), total protein, albumin, total bilirubin, direct bilirubin, and alkaline phosphatase (ALP) levels, will be measured in the venous blood samples. Proinflammatory (IL1-β, IL-6, TNFα, INF-γ) and anti-inflammatory (IL-2, IL-4, IL-10, IL-13) cytokines will be examined in venous blood in order to determine the immune modulatory effect of stem cells. CD4 + T, CD4 + T killer cells Granulocyte macrophage colony factor BLC-2 VEGF-R angiopoetin-1, angiopoetin-2 Total antioxidant capacity (TAC) Total oxidant capacity (TOC).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Pneumonia, Multiple Organ Failure, Corona Virus Infection
Keywords
Covid-19, Pneumonia, Multiple Organ Failure, Coronavirus, Mesenchymal stem cells, Cellular therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Untreated
Arm Type
No Intervention
Arm Description
Group 1: patients that are not on a ventilator (n=10) No extra intervention will be done.
Arm Title
Saline Control
Arm Type
Sham Comparator
Arm Description
Group 2: patients that are on a ventilator and will receive saline injections (n=10) as control for MSC transplantation group (3).
Arm Title
Experimental UC-MSCs
Arm Type
Experimental
Arm Description
Group 3: patients that are on a ventilator and will receive MSC transplantation injections (n=10)
Intervention Type
Biological
Intervention Name(s)
MSC Treatment
Intervention Description
Protocol length: 1 week Doses: Application: 3 million cells/kg IV-------------------------------------------------0 day Application: 3 million cells/kg IV ------------------------------------------------3rd day Application: 3 million cells/kg IV -------------------------------------------------6th day will be given to patients positively, clinically and radiologically diagnosed with COVID-19, followed with 3 months observation.
Intervention Type
Biological
Intervention Name(s)
Saline Control
Intervention Description
Saline will be given to patients positively, clinically and radiologically diagnosed with COVID-19, followed with 3 months observation.
Primary Outcome Measure Information:
Title
Clinical improvement
Description
Improvement of clinical symptoms related to Covid-19 infection (fever, pneumonia, shortness of breath)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Lung damage improvement
Description
Improvement of lungs assessed by CT Scan
Time Frame
3 months
Title
Sars-Cov-2 viral infection laboratory test
Description
Negative, measured by RT-PCR laboratory tests for the virus
Time Frame
3 months
Title
Blood test
Description
Cell types and numbers
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 40-60 years old male or female Confirmed 2019-nCoV infection with RT-PCR Laboratory test Confirmed Pneumonia with chest radiography and computer tomography and any of the following criteria: Shortness of breath (RR ≥30/min) Resting finger oxygen saturation 93% Arterial oxygen partial pressure (PaO2)/oxygen absorption concentration (FiO2) ≤ 300MMHG Advancing of focus in Pulmonary imaging to >50% in 24-48 hours Exclusion Criteria: Those who are not pregnant, breastfeeding and pregnant but who do not take effective contraceptive measures; Patients with malignant tumors, other serious systemic diseases and psychosis; Informed consent is not given or does not comply with the test requirements. Co-infection of HIV, tuberculosis, influenza virus, adenovirus and other respiratory infection virus. Pneumonia caused by bacteria, mycoplasma, chlamydia, legionella, fungi or co-infection of HIV, tuberculosis, influenza virus, adenovirus and other respiratory infection virus. Obstructive HABP / VABP caused by lung cancer or other known causes; Long-term history of use of immunosuppressive agents; History of epilepsy and need for continuous anticonvulsant therapy or anticonvulsant therapy taken within 3 years; Invasive ventilation Shock Other organ failures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gokhan T Adas, Prof.Dr.
Organizational Affiliation
SBÜ Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Erdal Karaoz, Prof.Dr.
Organizational Affiliation
Istinye University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istinye University
City
Istanbul
ZIP/Postal Code
34010
Country
Turkey
Facility Name
SBÜ Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi
City
Istanbul
ZIP/Postal Code
34147
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Clinical Use of Stem Cells for the Treatment of Covid-19

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