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Treatment for Coronavirus (CANCOV Trial)

N/A
Waitlist Available
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to 1,3,6 and 12 months. extension 18, 24, 30, 36, 42, 48, 54, 60 months.
Awards & highlights

Summary

The CANCOV study will be the first Canadian study to provide a comprehensive evaluation of early, and 1-year, outcomes of outpatient and hospitalized COVID-19 survivors and their family caregivers, their varied trajectories and associated clinical risk factors. The overall objectives are to determine short- (in hospital) and longer-term (1, 3, 6 and 12 months post-acute hospital discharge) outcomes COVID-19+ patients across the spectrum of symptom severity, including outpatients and inpatients from GIM and ICU wards and their caregivers, and the clinical, sociodemographic, multi-omic predictors of these outcomes. By leveraging expertise from investigators across disciplines and divisions, this study presents a suite of complementary projects that explore the genetic, transcriptomic, epigenomic and immunologic evaluation of COVID-19 infection across the illness and recovery trajectory during the acute illness and in the context of multidimensional long-term outcomes. As there continues to be need for longer term follow up and research on Long-COVID, this study has added an optional extension to include 2-year, 3-year, 4-year and 5 year outcomes.

Eligible Conditions
  • Coronavirus

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 1,3,6 and 12 months. extension 18, 24, 30, 36, 42, 48, 54, 60 months.
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to 1,3,6 and 12 months. extension 18, 24, 30, 36, 42, 48, 54, 60 months. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Secondary outcome measures
BORG Dypsnea scale
Care-giving Assistance Scale (CAS)
Care-giving Impact Scale (CIS)
+18 more

Find a Location

Who is running the clinical trial?

University Health Network, TorontoLead Sponsor
1,514 Previous Clinical Trials
498,029 Total Patients Enrolled
Unity HealthOTHER
3 Previous Clinical Trials
20,710 Total Patients Enrolled
The Hospital for Sick ChildrenOTHER
704 Previous Clinical Trials
6,954,701 Total Patients Enrolled
~735 spots leftby Dec 2026