Host Response Mediators in Coronavirus (COVID-19) Infection
NCT ID: NCT04510623
Last Updated: 2020-08-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
500 participants
OBSERVATIONAL
2020-03-17
2022-06-30
Brief Summary
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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.
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Detailed Description
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Main Hypothesis: Modulation of ACE2 by ARBs decreases the need for hospitalization, severity (need for ventilation, vasopressors, extracorporeal membrane oxygenation or renal replacement therapy) or mortality of hospitalized COVID-19 infected adults.
Secondary Hypotheses:
* Plasma angiotensin I and II and other biomarker levels are associated with effectiveness of ARBs in hospitalized COVID-19 adults
* Modulation of ACE2 by angiotensin type I receptor blockers is associated with decreased rate of hospitalization for COVID-19
* In patients already on ARBs when they are hospitalized continuing ARBs is associated with decreased World Health Organization (WHO) COVID-19 ordinal outcome scale
Justification: The COVID-19 epidemic continues to grow exponentially affecting over 71,429 individuals with 1775 deaths (February 17, 2020), mostly in China but also in other countries. The population mortality rate is 2% (lower than SARS (10%) and MERS (36%) but is 10% in hospitalized and 24% in ICU-admitted COVID-19 patients in China. Recent data from China (not yet public domain) suggest ICU mortality is higher (J. Marshall personal communication). Interventions to date include quarantine, isolation and usual clinical care. There are no proven antiviral or host modulating interventions for COVID-19. Notably, critically ill COVID-19 patients have similar mortality rates as sepsis and acute respiratory distress syndrome. Cohort studies have shown that patients already on angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) have lower sepsis mortality. Angiotensin II worsens lung injury in influenza models because ACE2 is downregulated in H1N1, H5N1, H7N9, and SARS viral infections leading to increased angiotensin II. Angiotensin II levels are increased in human influenza and are associated with influenza viral load, disease progression and mortality. Preliminary data shows 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.
Research Design:
Prospective clinical chart review: we will collect clinical data on the participant throughout their hospital stay. Includes collection of baseline characteristics such as age, sex, heart rate, respiratory rate, temperature, blood pressure, SaO2, respiratory (PaO2/FiO2), renal (creatinine) and hepatic (bilirubin) function, use of oxygen, vasopressors, ventilation and RRT. They will be followed daily throughout their hospital stay, until death or discharge. Using left over clinical blood collected upon admission to hospital, plasma angiotensin I and II and other biomarker levels will be measured in our research laboratories.
Conditions
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Study Design
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COHORT
OTHER
Study Groups
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COVID-19 Patients on ARBs
This is an observational cohort study. Those who have COVID-19 in hospital and are on Angiotensin Receptor Blockers will be included in this cohort.
ARBs and/or ACE inhibitors
This is an observational study only.
COVID-19 Patients on ACE inhibitors
This is an observational cohort study. Those who have COVID-19 in hospital and are on Angiotensin-Converting Enzyme inhibitors will be included in this cohort.
ARBs and/or ACE inhibitors
This is an observational study only.
COVID-19 Patients on ARBs or ACE inhibitors
This is an observational cohort study. Those who have COVID-19 in hospital and are on ARBs or ACEi's will be included in this cohort.
ARBs and/or ACE inhibitors
This is an observational study only.
COVID-19 Patients not on ARBs or ACE inhibitors
This is an observational cohort study. Those who have COVID-19 in hospital and are not on ARBs or ACEi's will be included in this cohort.
Usual Care
This is an observational study only.
Interventions
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ARBs and/or ACE inhibitors
This is an observational study only.
Usual Care
This is an observational study only.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Canadian Institutes of Health Research (CIHR)
OTHER_GOV
British Columbia Centre for Disease Control
OTHER_GOV
McGill University Health Centre/Research Institute of the McGill University Health Centre
OTHER
University of Toronto
OTHER
University of Ottawa
OTHER
University of Calgary
OTHER
University of Alberta
OTHER
University of Victoria
OTHER
Wuhan University
OTHER
Peking Union Medical College
OTHER
University of Pennsylvania
OTHER
University of British Columbia
OTHER
Responsible Party
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Jim Russell
Study-Wide Principal Investigator
Principal Investigators
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James A Russell, MD
Role: PRINCIPAL_INVESTIGATOR
St Paul's Hospital, Center for Heart and Lung Innovation
Locations
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University of Calgary - Foothills
Calgary, Alberta, Canada
Stollery Children's Hospital
Edmonton, Alberta, Canada
University of Alberta
Edmonton, Alberta, Canada
Surrey Memorial Hospital
Surrey, British Columbia, Canada
St Pauls Hospital
Vancouver, British Columbia, Canada
Vancouver General Hospital
Vancouver, British Columbia, Canada
William Osler Health System
Brampton, Ontario, Canada
Queens University
Kingston, Ontario, Canada
Humber River Hospital
North York, Ontario, Canada
Mount Sinai Hospital
Toronto, Ontario, Canada
St Michael's Hospital
Toronto, Ontario, Canada
Sunnybrook Hospital
Toronto, Ontario, Canada
Jewish General Hospital
Montreal, Quebec, Canada
McGill University Health Center
Montreal, Quebec, Canada
Université de Sherbrooke
Sherbrooke, Quebec, Canada
Countries
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Central Contacts
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Facility Contacts
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Brent Winston, MD
Role: primary
Ari Joffe, MD
Role: primary
Oleksa Rewa, MD
Role: primary
Gregory Haljan, MD
Role: primary
David Sweet, MD
Role: primary
David Maslove, MD
Role: primary
Nataly Farshait
Role: primary
Allison McGeer, MD
Role: primary
John Marshall, MD
Role: primary
Robert Fowler, MD
Role: primary
Todd Lee, MD
Role: primary
Matthew Cheng, MD
Role: primary
Francois Lamontagne, MD
Role: primary
References
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Lee T, Cheng MP, Vinh DC, Lee TC, Tran KC, Winston BW, Sweet D, Boyd JH, Walley KR, Haljan G, McGeer A, Lamontagne F, Fowler R, Maslove D, Singer J, Patrick DM, Marshall JC, Burns KD, Murthy S, Mann PK, Hernandez G, Donohoe K, Rocheleau G, Russell JA; ARBs CORONA I study investigators. Organ dysfunction and death in patients admitted to hospital with COVID-19 in pandemic waves 1 to 3 in British Columbia, Ontario and Quebec, Canada: a cohort study. CMAJ Open. 2022 Apr 19;10(2):E379-E389. doi: 10.9778/cmajo.20210216. Print 2022 Apr-Jun.
Russell JA, Marshall JC, Slutsky A, Murthy S, Sweet D, Lee T, Singer J, Patrick DM, Du B, Peng Z, Cheng M, Burns KD, Harhay MO. Study protocol for a multicentre, prospective cohort study of the association of angiotensin II type 1 receptor blockers on outcomes of coronavirus infection. BMJ Open. 2020 Dec 7;10(12):e040768. doi: 10.1136/bmjopen-2020-040768.
Other Identifiers
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H20-00600
Identifier Type: -
Identifier Source: org_study_id
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