IRCM Post-COVID-19 (IPCO) Research Clinic: a Multidisciplinary Approach to Evaluate Short and Long-term Complications of COVID-19

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Design: This is a prospective, observational cohort study to evaluate the short- and long-term end-organ complications of COVID-19 and to establish a COVID-19 biobank. Participant Cohorts: 1. Individuals who had previous asymptomatic or mild COVID-19 (mild=never required supplemental oxygen during the acute phase of the infection) 2. Individuals who had previous moderate or severe COVID-19 (moderate=required supplemental oxygen by nasal cannula during the acute phase of the infection; severe=required supplemental oxygen by either high-flow nasal cannula, non-invasive positive pressure ventilation or intubation) 3. Individuals who had COVID-19 but did not have signs or symptoms related to COVID-19 lasting beyond 4 weeks from the date of COVID-19 symptom-onset or diagnosis 4. Individuals who have not had COVID-19 (i.e. individuals who tested negative for COVID-19 and who never had symptoms consistent with COVID-19)

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: t
View:

• Any gender, ≥ 18 years old

• Current resident of Quebec

• Speaks English or French

• Have a personal email (to which to send reminders and questionnaire by email )

⁃ AND

⁃ 1 of the following criteria:

• At least one COVID-19 positive PCR test, serology or antibody/antigen test in the last 24 months at day of recruitment.

• In the absence of a positive COVID-19 test, the patient had symptoms consistent with COVID-19 while living with a person who had a confirmed positive PCR/serology COVID-19 test.

• Individual who tested negative for COVID-19 while living with a household member who tested positive for COVID-19 (control group), and never had any COVID-19 related symptoms.

• Individual who doesn't have any COVID-19 related symptoms actually, has never had tested positive, and has had at least one negative PCR test.

Locations
Other Locations
Canada
Institut de Recherches Cliniques de Montreal
RECRUITING
Montreal
Contact Information
Primary
Emilia Liana Falcone, M.D., Ph.D.
Emilia.falcone@ircm.qc.ca
514-987-5610
Backup
Charlotte Du Sablon, M.Sc.
Charlotte.Dusablon@ircm.qc.ca
514-987-5581
Time Frame
Start Date: 2021-01-01
Estimated Completion Date: 2027-11-04
Participants
Target number of participants: 570
Treatments
COVID-19 positive patients
1. Patients who had previous asymptomatic or mild COVID-19 (mild=never required supplemental oxygen during the acute phase of the infection)~2. Patients who had previous moderate or severe COVID-19 (moderate=required supplemental oxygen by nasal cannula during the acute phase of the infection; severe=required supplemental oxygen by either high-flow nasal cannula, non-invasive positive pressure ventilation or intubation~3. Patients who had COVID-19 but did not have signs or symptoms related to COVID-19 lasting beyond 4 weeks from the date of COVID-19 symptom-onset or diagnosis
COVID-19 negative patients
Patients who have not had COVID-19 (i.e., patients who tested negative for COVID-19 and who never had symptoms consistent with COVID-19)
Sponsors
Leads: Emilia Falcone, MD

This content was sourced from clinicaltrials.gov