Host Response Mediators in Coronavirus (COVID-19) Infection

NCT ID: NCT04510623

Last Updated: 2020-08-12

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-03-17

Study Completion Date

2022-06-30

Brief Summary

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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.

Detailed Description

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Purpose: To determine whether angiotensin II receptor blockers (ARBs) decrease severity or mortality in hospitalized COVID-19 infected adults.

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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COVID-19 SARS-CoV2

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

Intervention Type OTHER

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

Intervention Type OTHER

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

Intervention Type OTHER

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

Intervention Type OTHER

This is an observational study only.

Interventions

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ARBs and/or ACE inhibitors

This is an observational study only.

Intervention Type OTHER

Usual Care

This is an observational study only.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Individuals over 18 years of age who have confirmed COVID-19 infection (according to local hospital or provincial laboratories clinically approved laboratory testing for COVID-19).

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Canadian Institutes of Health Research (CIHR)

OTHER_GOV

Sponsor Role collaborator

British Columbia Centre for Disease Control

OTHER_GOV

Sponsor Role collaborator

McGill University Health Centre/Research Institute of the McGill University Health Centre

OTHER

Sponsor Role collaborator

University of Toronto

OTHER

Sponsor Role collaborator

University of Ottawa

OTHER

Sponsor Role collaborator

University of Calgary

OTHER

Sponsor Role collaborator

University of Alberta

OTHER

Sponsor Role collaborator

University of Victoria

OTHER

Sponsor Role collaborator

Wuhan University

OTHER

Sponsor Role collaborator

Peking Union Medical College

OTHER

Sponsor Role collaborator

University of Pennsylvania

OTHER

Sponsor Role collaborator

University of British Columbia

OTHER

Sponsor Role lead

Responsible Party

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Jim Russell

Study-Wide Principal Investigator

Responsibility Role 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

Site Status RECRUITING

Stollery Children's Hospital

Edmonton, Alberta, Canada

Site Status RECRUITING

University of Alberta

Edmonton, Alberta, Canada

Site Status RECRUITING

Surrey Memorial Hospital

Surrey, British Columbia, Canada

Site Status NOT_YET_RECRUITING

St Pauls Hospital

Vancouver, British Columbia, Canada

Site Status RECRUITING

Vancouver General Hospital

Vancouver, British Columbia, Canada

Site Status RECRUITING

William Osler Health System

Brampton, Ontario, Canada

Site Status RECRUITING

Queens University

Kingston, Ontario, Canada

Site Status RECRUITING

Humber River Hospital

North York, Ontario, Canada

Site Status RECRUITING

Mount Sinai Hospital

Toronto, Ontario, Canada

Site Status RECRUITING

St Michael's Hospital

Toronto, Ontario, Canada

Site Status NOT_YET_RECRUITING

Sunnybrook Hospital

Toronto, Ontario, Canada

Site Status NOT_YET_RECRUITING

Jewish General Hospital

Montreal, Quebec, Canada

Site Status RECRUITING

McGill University Health Center

Montreal, Quebec, Canada

Site Status RECRUITING

Université de Sherbrooke

Sherbrooke, Quebec, Canada

Site Status RECRUITING

Countries

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Canada

Central Contacts

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Puneet Mann, MSc

Role: CONTACT

604 682 2344 ext. 64734

Lynda Lazosky

Role: CONTACT

604-682-2344 ext. 64886

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

Puneet Mann, MSc

Role: primary

604 682 2344 ext. 64734

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.

Reference Type DERIVED
PMID: 35440485 (View on PubMed)

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.

Reference Type DERIVED
PMID: 33293316 (View on PubMed)

Other Identifiers

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H20-00600

Identifier Type: -

Identifier Source: org_study_id

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