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International Severe Asthma Registry: Canadian Cohort

Severe Asthma

The International Severe Asthma Registry is a global initiative looking to ensure that the care of people with severe asthma will continue to improve by collecting detailed information about the health and treatment of as many people with the disease as possible. The study will gather anonymized longitudinal real-life data for participants with severe asthma for five years. The purpose of the registry is to track the progress of participants and determine how well they are responding to treatment. Medical research using data from the registry will give the investigators a better understanding of severe asthma and help the investigators develop and improve the care and treatment for severe asthma participants. The Canadian cohort of the registry will collect information from Canadian participants with severe asthma across seven different sites.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

* Participants 18 years or older
* Participants receiving treatment according to GINA Step 5 or uncontrolled in GINA Step 4 (uncontrolled is defined as having severe asthma symptoms or frequent exacerbations)

Exclusion Criteria:

-Participants with mild to moderate asthma

Lieu de l'étude

University of Alberta
University of Alberta
Edmonton, Alberta
Canada

Contactez l'équipe d'étude

Primary Contact

Amy Haarsma

[email protected]
(780) 492-3741
Kingston General Hospital
Kingston General Hospital
Kingston, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Alison Morra

[email protected]
McGill University
McGill University
Montréal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Cathy Fugere

[email protected]
(514) 934-1934
University of British Columbia
University of British Columbia
Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Primary Contact

Leiana Hoshyari

[email protected]
(604) 682-2344
Inspiration Research Limited
Inspiration Research Limited
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Kayla Cardoso

[email protected]
(416) 944-9602
University of Saskatchewan
University of Saskatchewan
Saskatoon, Saskatchewan
Canada

Contactez l'équipe d'étude

Synergy MD Specialty Group
Synergy MD Specialty Group
Edmonton, Alberta
Canada

Contactez l'équipe d'étude

Primary Contact

Carrie McPhee

[email protected]
University of Western Ontario
University of Western Ontario
London, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Hana Serajeddini

[email protected]
Université Laval
Université Laval
Quebéc City, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Marie-Eve Boulay

[email protected]
(418) 656-8711
University of British Columbia
University of British Columbia
Vancouver, British Columbia
Canada

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Primary Contact

Shelley Abercromby

[email protected]
(604) 875-4111
The Ottawa Hospital
The Ottawa Hospital
Ottawa, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Kathy Vandemheen

[email protected]
(613) 737-8259
Université de Sherbrooke
Université de Sherbrooke
Sherbrooke, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Martine Duval

[email protected]
Étude parrainée par
University of British Columbia
Participants recherchés
Plus d'informations
ID de l'étude: NCT04045587