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The Ontario Multi-Regional Hospital COVID-19 Registry (COREG)- Recovery Trajectory Sub-study

The Ontario Multi-Regional Hospital COVID-19 Registry (COREG)- Recovery Trajectory Sub-study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04868864
Acronym
COREG
Enrollment
200
Registered
2021-05-03
Start date
2021-05-15
Completion date
2022-12-31
Last updated
2021-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19 Pneumonia, Sars-CoV-2 Infection

Brief summary

Radiological and lung function recovery following Covid-19 infection.

Detailed description

The investigators propose to conduct pulmonary LDCT imaging and physiological lung function assessments, and combine this with detailed multi-regional hospitalization clinical data collection on COVID-19 cases (COREG registry); to inform long-term pulmonary and extra-pulmonary consequences and the recovery trajectory following COVID-19 infection.

Interventions

DIAGNOSTIC_TESTCT scan

Non-enhanced LDCT scans of the thorax will be taken using standard technology on helical CT system

DIAGNOSTIC_TESTPulmonary Function Test

Standard pulmonary function testing will be conducted by trained pulmonary technologists following the American Thoracic Society standards

Sponsors

Gilead Sciences
CollaboratorINDUSTRY
Hamilton Health Sciences Corporation
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients discharged from hospital post COVID-19 infection who have radiographic and clinical evidence of COVID-19 pneumonia during hospitalization. * Patients with evidence of unresolved radiographic changes or persistent hypoxemia.

Exclusion criteria

* Failure to comply with study procedures.

Design outcomes

Primary

MeasureTime frameDescription
Pulmonary changes on LDCT ScanThrough study completion, an average of 9 monthsIdentify pulmonary changes utilizing LDCT chest to characterize the pulmonary recovery trajectory of survivors of COVID-19.

Secondary

MeasureTime frameDescription
DLCOThrough study completion, an average of 9 monthsIdentify DLCO changes over time to characterize the pulmonary recovery trajectory of survivors of COVID-19.
TLCThrough study completion, an average of 9 monthsIdentify TLC changes over time to characterize the pulmonary recovery trajectory of survivors of COVID-19.
FEV1Through study completion, an average of 9 monthsIdentify FEV1 changes over time to characterize the pulmonary recovery trajectory of survivors of COVID-19.
FVCThrough study completion, an average of 9 monthsIdentify FVC changes over time to characterize the pulmonary recovery trajectory of survivors of COVID-19.

Countries

Canada

Contacts

Primary ContactMylinh Duong, MD
duongmy@mcmaster.ca905 525-9140

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026