UVA Light Device to Treat COVID-19
Purpose
This pilot study will assess the safety and effectiveness of UV light treatment in hospitalized patients with COVID-19.
Condition
- Coronavirus
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Confirmed positive test result for SARS-CoV-2 - Mechanically ventilated - Endotracheal tube inner diameter of at least 7.5 mm
Exclusion Criteria
- Unable to provide informed consent (or surrogate) - Enrolled in a therapeutic clinical trial for same condition that does not allow recruitment in other trials - Pregnant women
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Intervention Model Description
- Intubated patients with confirmed SARS-CoV-2 will receive UV light treatment to potentially reduce bacterial and viral burden.
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Endotracheal UV Light |
Mechanically ventilated patients who will receive UV Light therapy |
|
Recruiting Locations
More Details
- NCT ID
- NCT04572399
- Status
- Completed
- Sponsor
- Cedars-Sinai Medical Center
Detailed Description
This is a single center, open label, pilot study. 5 adult patients, aged over 18, who are confirmed positive with SARS-CoV-2 and are newly intubed, will receive UV light treatment to reduce SARS-CoV-2 viral load.