Official Title
Respiratory Application of a Novel Ultraviolet Light Delivery Device for Patients Infected With COVID-19: A Pilot Study
Brief Summary

This pilot study will assess the safety and effectiveness of UV light treatment in hospitalized patients with COVID-19.

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.

Completed
Coronavirus

Device: UV Light Treatment

UV light therapy administered while patient is mechanically ventilated

Eligibility Criteria

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

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United States
Locations

Cedars-Sinai Medical Center
Los Angeles, California, United States

George Chaux, MD, Principal Investigator
Cedars-Sinai Medical Center

Aytu BioPharma, Inc.
NCT Number
MeSH Terms
Coronavirus Infections