Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:49 AM
Ignite Modification Date:
2025-12-25 @ 3:49 AM
NCT ID:
NCT04796402
Eligibility Criteria:
Inclusion Criteria:
1. Age at the time of SARS-CoV2 test:
1. Age \> 65
2. Age 55-64 and 1 or more of:
i. BMI\>35, ii. chronic kidney disease, iii. diabetes mellitus, iv. immunosuppressive disease v. current immunosuppressive treatment vi. hypertension vii. coronary artery disease viii. chronic lung disease
c. Age 18-54 and 1 or more of: i. BMI\>35 ii. chronic kidney disease iii. diabetes mellitus iv. immunosuppressive disease v. current immunosuppressive treatment
2. Disease Characteristics:
1. Not hospitalized
2. Sample collection for first SARS-CoV2 test positive within 3 days prior to consent.
3. One or more mild COVID-19 symptoms and within 10 days from onset
i. Fever ii. Cough iii. Sore throat iv. Malaise v. Headache vi. Muscle pain vii. Gastrointestinal symptoms viii. Shortness of breath with/without exertion
3. Study Procedures:
1. Resident of British Columbia
2. Understand and agree to planned study procedures
4. Ability and Willingness to Provide Informed Consent:
The participant will provide informed consent by telephone
Exclusion Criteria:
1. Medical Conditions
1. Allergies to any of the components used in the formulation of the bamlanivimab
2. Hospitalization or expected to need hospitalization in the next 24 hours at the time of recruitment for COVID-19
3. Suspected or proven infection other than COVID-19 that in the opinion of the clinicians could pose a risk to study inclusion
4. Any co-morbidity considered life-threatening in \<28 days, or requiring surgery in \<7 days.
5. Any serious disease, condition or disorder that in the opinion of the clinicians should preclude participation.
6. Require oxygen therapy due to COVID-19
7. Require an increase in baseline oxygen flow rate due to COVID-19 in those on chronic oxygen therapy due to underlying non-COVID-19 related comorbidity.
2. Weighs \< 40 kg
3. History of vaccination against SARS-CoV2
4. History of convalescent plasma or IVIG therapy within 3 months of first SARS-CoV2 viral determination positive
5. History of previous SARS-CoV2 infection
6. History of participation in any clinical study involving an investigational intervention within 30 days or 5 half-lives of the previous intervention, whichever is longer.
7. Unable to achieve informed consent for any reason
8. Known Pregnancy
9. Actively breast-feeding.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04796402
Study Brief:
Protocol Section:
NCT04796402