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Mesenchymal Stem Cells Therapy in Patients With COVID-19 Pneumonia

K

Kanuni Sultan Suleyman Training and Research Hospital

Status

Completed

Conditions

Coronavirus Disease 2019 (COVID-19) Pneumonia

Treatments

Other: Mesenchymal stem cells

Study type

Interventional

Funder types

Other

Identifiers

NCT04713878
2020.05.20

Details and patient eligibility

About

Due to the cytokine storm that develops as a result of Coronavirus Disease 2019 (COVID-19) infection, some patients hospitalization to intensive care cause of pneumonia, Acute Respiratory Distress Syndrome (ARDS) and multiple organ failure. Mortality is higher in treatment-resistant cases.

Purpose of this study:

  1. Providing immune modulation by Stem Cell Transplantation and reducing the damage caused by cytokine storm to tissues and organs,
  2. Correcting immunosuppression and fight against COVID-19 virus by editing B and T cells,
  3. It is to accelerate healing in organ damage by increasing growth factors through mesenchymal stem cells.

Primary outcome: Improvement of clinical symptoms, reduction of cytokine storm Secondary outcome: Recovery of patients; from mechanical ventilation

Full description

Study design and participants This study was a single-center open-label, randomized trial conducted at an Education and Training Hospital, Istanbul from May to July, 2020, and it was performed according to the Declaration of Helsinki and approved by the Ethics Committee and health ministry (No:2020.05.20). Written informed consent was obtained from all patients or their representatives when data were collected prospectively.

Age, gender, mortality status, APACHE II score, number of days in ICU, procalcitonin and C-reactive protein values, leukocyte values, comorbid diseases, The cluster of differentiations 4 and 8 (CD4 and CD8), interleukin -2, interleukin -6, Tumor necrosis factor-alpha-beta levels will be recorded.

Clinical results, changes in inflammatory and immune function levels, and side effects will be recorded. The patient's lung function and symptoms will be recorded after Mesenchymal Stem Cell transplantation. After treatment, lymphocyte, C-reactive protein, Tumor Necrosis alpha-beta levels , interleukin-6 levels will be recorded.

Patients were divided into 3 groups:

  1. group: Intubated without comorbidity (n:7)
  2. group: Intubated with comorbidity (n:7)
  3. group: No intubated (n:7)

Dosage of Mesenchymal stem cells:

  1. 1 million cell/kg iv--------------------------------------------------day 0
  2. 1 million cell/kg iv -------------------------------------------------day 2
  3. 1 million cell/kg iv -------------------------------------------------day 4

Enrollment

21 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged 18-90 male or female
  • laboratory approve of RT-PCR (real-time reverse transcription polymerase chain reaction) with COVID-19 infection
  • pneumonia assessed by chest radiography or computed tomography
  • In accordance with any of the following: 1)Respiratory rate ≥ 30 times / min 2) oxygen saturation ≤ 93% 3) arterial pressure of oxygen/the fraction of inspired oxygen≤ 300mmHg, 4) pulmonary imaging of focus within 24-48 hours > 50% progression
  • patients who remain unresponsive to medications administered according to Ministry of health guidelines
  • Patients who receiving invasive or non-invasive mechanical ventilation therapy in intensive care

Exclusion criteria

  • Pregnancy
  • Any kind of cancer, severe liver disease
  • Failure to provide informed consent or comply with test requirements
  • Known allergy or hypersensitivity to MSCs

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

21 participants in 3 patient groups

Group 1
Active Comparator group
Description:
Intubated without comorbidity
Treatment:
Other: Mesenchymal stem cells
Group 2
Active Comparator group
Description:
Intubated with comorbidity
Treatment:
Other: Mesenchymal stem cells
Group 3
Active Comparator group
Description:
No intubated
Treatment:
Other: Mesenchymal stem cells

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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