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Completed

NCT Number: NCT04451291

Study of Decidual Stromal Cells to Treat COVID-19 Respiratory Failure

This is a research study to see how safe and effective decidual stromal cells are in treating patients with respiratory failure (breathing problem where not enough oxygen is passed from the lungs into the blood) caused by COVID-19.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Brampton Civic Hospital, Brampton, Ontario, Canada

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About this study

COVID-19 viral infectious disease that has lead to high numbers of critically ill patients or death due to respiratory failure.

Decidual Stromal Cells (DSC) may be useful in the treatment of acute respiratory distress syndrome (ARDS) by reducing lung inflammation and then time that patients require help with breathing (mechanical ventilation).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Able to provide informed consent for participation in the study, either by the participant themselves or by the legally acceptable representative (LAR)
  • Virological diagnosis of SARS-CoV-2 infection (PCR)
  • Acute respiratory distress syndrome (ARDS) not due to cardiac causes
  • Receiving mechanical ventilation

Exclusion criteria

  • Severe comorbidity with life expectancy <3 months according to investigators assessment
  • Currently receiving extracorporeal membrane oxygenation (ECMO)
  • Patients with established positive bacterial blood cultures prior to enrollment or suspicion of superimposed bacterial pneumonia
  • Patients with diagnosed significant pulmonary embolism or deep vein thrombosis in the previous 3 months
  • Patients who have been intubated for more than 48 hours
  • Known hypersensitivity to dimethyl sulfoxide (DMSO) or to porcine or bovine proteins
  • Acute co-morbidity within 7 days before inclusion such as stroke
  • History of severe chronic history of heart disease, recent myocardial infarction or unstable angina, lung disease (requiring home oxygen), pulmonary hypertension, or liver comorbidities
  • Malignancy that requires treatment in the previous two years (excluding non-melanoma skin malignancies treated by excision, or cryotherapy)
  • History of immunosuppression (immunomodulators or anti-rejection drugs in past year, or active disease, autoimmune disease on treatment, transplant recipients) or anaphylaxis
  • Refusal of blood products
  • Severe co-morbidity/co-morbidities which in the opinion of the investigators would compromise safety assessments
  • Pregnant or breast-feeding
  • Actively participating on another trial of an investigational agent for ARDS
  • Unacceptable laboratory blood tests for alanine aminotransferase (ALT)/aspartate aminotransferase (AST), neutrophils, or platelets

Treatment and study plan

Decidual stromal cells (DSC)

Biological

DSCs are involved in the immune system during pregnancy. The DSCs used in this study will come from laboratory grown allogeneic human decidual stromal cells obtained from donated placentas.

Primary outcomes

  1. Number of ventilator free days following infusion of decidual stromal cells

    Time frame: 28 days

Secondary outcomes

  1. Mortality rate from COVID-19

    Time frame: 28 days

  2. Mortality rate from COVID-19

    Time frame: 60 days

  3. Mortality rate from COVID-19

    Time frame: 180 days

  4. All-cause morality rate

    Time frame: 28 days

  5. All-cause morality rate

    Time frame: 60 days

  6. All-cause morality rate

    Time frame: 180 days

  7. Average number of days in ICU

    Time frame: 180 days

  8. Average number of days of hospital admittance

    Time frame: 180 days

  9. Average days not requiring vasopressors

    Time frame: 180 days

  10. Overall survival rate

    Time frame: 180 days

  11. Average viral clearance

    Time frame: 180 days

  12. Average number of days of supplemental oxygenation

    Time frame: 180 days

  13. Average number of day without supplemental oxygen

    Time frame: 180 days

  14. Mean PaO2/FiO2 as compared to patient baseline

    Time frame: 180 days

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Collaborators

  • Oslo University Hospital

Registry information

Official study title

DSC-COVID-19: An Open-label Study on the Safety and Efficacy of Decidual Stromal Cells in Respiratory Failure Induced by COVID-19

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Jun 30, 2020
Registry last updated
Feb 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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