Coronavirus Clinical Trial
Official title:
Respiratory Application of a Novel Ultraviolet Light Delivery Device for Patients Infected With COVID-19: A Pilot Study
NCT number | NCT04572399 |
Other study ID # | 883 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 30, 2020 |
Est. completion date | December 28, 2020 |
Verified date | January 2022 |
Source | Cedars-Sinai Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This pilot study will assess the safety and effectiveness of UV light treatment in hospitalized patients with COVID-19.
Status | Completed |
Enrollment | 5 |
Est. completion date | December 28, 2020 |
Est. primary completion date | December 28, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | Cedars-Sinai Medical Center | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
Cedars-Sinai Medical Center | Aytu BioPharma, Inc. |
United States,
Rezaie A, Melmed GY, Leite G, Mathur R, Takakura W, Pedraza I, Lewis M, Murthy R, Chaux G, Pimentel M. Endotracheal Application of Ultraviolet A Light in Critically Ill Patients with Severe Acute Respiratory Syndrome Coronavirus 2: A First-in-Human Study. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Viral Load | Change of viral load in upper airway in patients admitted to hospital for COVID-19 | 5 days | |
Secondary | Change in Bacterial Load | Change of bacterial load in upper airway | 5 days | |
Secondary | Ventilated Associated Pneumonia | Percentage of patients developing ventilated pneumonia (VAP) within 30 days of treatment | 1 month | |
Secondary | Days to Extubation | Number of days patient is intubated with endotracheal tube or tracheostomy | 1 month | |
Secondary | Days to Discharge | Number of days patient is discharged from the hospital | 1 month | |
Secondary | Change in C-reactive Protein | Change in C-reactive protein from baseline to the end of the treatment | 5 days | |
Secondary | Change in the World Health Organization (WHO) Coronavirus Disease (COVID)-19 10-point Ordinal Severity Scale by 30 Days | The World Health Organization (WHO) COVID-19 10-point ordinal severity scale:
0 uninfected, No viral RNA detected Asymptomatic; viral RNA detected Ambulatory Mild disease: Symptomatic; independent Ambulatory Mild disease: Symptomatic; assistance needed Hospitalized: Moderate disease; no oxygen therapy Hospitalized: Moderate disease; oxygen by mask or nasal prongs Hospitalized: sever disease, Oxygen by non-invasive ventilation or high flow Hospitalized: severe disease, intubation and mechanical ventilation, pO2/FiO2>=150 or SpO2/FiO2>=200 Hospitalized: severe disease, Mechanical ventilation pO2/FiO2<150(SpO2/FiO2 <200) or vasopressors Hospitalized: severe disease, Mechanical ventilation pO2/FiO2<150 and vasopressors, dialysis or extracorporeal membrane oxygenation Death |
1 month | |
Secondary | Catheter Tip Assessment on the Last Day of Treatment | Assessment of total bacterial load on the UV catheter tip on the last day of treatment | 5 days |
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