Host Response Mediators in Coronavirus (COVID-19) Infection

NCT04510623 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2020-08-12

No results posted yet for this study

Summary

The coronavirus (COVID-19) pandemic continues to grow exponentially. Angiotensin II levels are increased in human influenza and are associated with influenza viral load, disease progression and mortality. Preliminary data shows angiotensin II receptor blockers (ARBs) limits lung injury in murine influenza H7N9, as well as viral titre and RNA. ARBs could limit viral titre and organ injury in COVID-19. We will therefore collect clinical chart data and test angiotensin II levels of patients who are admitted to ICU with COVID-19 to determine whether there is a correlation between taking ARBs and clinical outcomes in these patients.

Other blood biomarkers and clinical risk factors for COVID-19 have come to light in recent weeks. We include these in our observational analysis to help generate an understanding of COVID-19 presentation and blood biomarker characterization of disease.

Conditions

Interventions

OTHER

ARBs and/or ACE inhibitors

This is an observational study only.

OTHER

Usual Care

This is an observational study only.

Sponsors & Collaborators

  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • British Columbia Centre for Disease Control

    collaborator OTHER_GOV
  • McGill University Health Centre/Research Institute of the McGill University Health Centre

    collaborator OTHER
  • University of Toronto

    collaborator OTHER
  • University of Ottawa

    collaborator OTHER
  • University of Calgary

    collaborator OTHER
  • University of Alberta

    collaborator OTHER
  • University of Victoria

    collaborator OTHER
  • Wuhan University

    collaborator OTHER
  • Peking Union Medical College

    collaborator OTHER
  • University of Pennsylvania

    collaborator OTHER
  • University of British Columbia

    lead OTHER

Principal Investigators

  • James A Russell, MD · St Paul's Hospital, Center for Heart and Lung Innovation

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-17
Primary Completion
2021-06-30
Completion
2022-06-30

Countries

  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04510623 on ClinicalTrials.gov