London's Exogenous Surfactant Study for COVID19

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's20 enrolled

Overview

The research team is investigating administering exogenous surfactant in COVID-19 patients with ARDS. The overall goal is to improve the outcome (mortality) of mechanically ventilated COVID-19 patients. Although the investigators anticipate that clinical outcomes may improve in the small group of patients receiving exogenous surfactant therapy in this small, single center study, the primary goal is to first determine feasibility and safety.

The most severe patients infected by the virus that causes COVID-19 develop severe respiratory failure (called ARDS) and require mechanical ventilation in the intensive care unit to help maintain oxygen delivery to the blood. Often these patients further deteriorate while on mechanical ventilation. This trial will determine the feasibility and safety of a therapy that can potentially improve lung function, reduce the need for mechanical ventilation and hopefully impact mortality. Adult patients with COVID-19 induced respiratory failure will be randomly assigned to receive either standard treatment or standard treatment plus exogenous surfactant. If enrolled in the latter, exogenous surfactant will be instilled into the lungs within 48 hours of intubation. The study is founded on extensive research on ARDS for over 30 years, leading to evidence suggesting that exogenous surfactant administration may be beneficial in this disease. Importantly, exogenous surfactant is already utilized all over the world to reduce mortality in preterm infants. When tested in adults with ARDS, it was shown to be well tolerated and safe. Furthermore, clinical and laboratory evidence suggests that this therapy may be most effective in patients with a direct lung infection, and when administered shortly after the patient is intubated. In this study, twenty patients who are proven COVID-19 positive and require MV due to progressive respiratory failure will be randomized to receive either 1) exogenous surfactant (BLES) as soon as possible and within 48 hours of intubation and stabilization, or 2) treatment as usual (will not be treated with surfactant). The overall goal is to improve the outcome (mortality) of mechanically ventilated COVID-19 patients. Although the investigators anticipate that clinical outcomes may improve in the small group of patients receiving exogenous surfactant therapy in this small, single center study, the primary goal is to first determine feasibility and safety. Should the investigators obtain promising results, the data obtained from this study will be used to develop a large trial to test the impact of this therapy on the clinical outcomes, including mortality, associated with COVID-19.

Study Type

INTERVENTIONAL

Conditions

ARDS, Human COVID-19

Interventions

Bovine Lipid Extract SurfactantDRUG

BLES will be administered in doses of 50mg/kg ideal bodyweight, at a concentration of 27mg/ml so a total volume of approximately 2ml/kg will be administered. The material will be instilled via the suction catheter through the ET tube so that the ventilation circuit is not broken. Half of the material will be instilled with the patient positioned on their left and right sides, with a pause to allow 5 min of MV between. The procedure will be repeated at, 24 and 48 hours while intubated, so the patient will receive up to 3 doses. To minimize aerosol generation, all patients will be paralyzed during surfactant administration and the ventilator will be paused. The proposed administration technique, surfactant concentration, volume and dosing schedule is based on previous studies, and has shown to be safe in patients with ARDS.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. age over 18 years 2. definitive proof of COVID-19 infection within 48 hours of intubation 3. acute respiratory failure with PaO2/FiO2 \< 300 requiring intubation Exclusion Criteria: 1. known or high suspicion of pre-existing heart failure, unstable angina 2. presence of severe shock with hemodynamic instability despite escalating vasopressors 3. severe, underlying lung disease (COPD, pulmonary fibrosis, lung cancer. etc.) 4. Concurrent treatments are delivered directly into the lung (ie anesthetics etc) 5. Diagnosis of pulmonary hemorrhage

Locations (2)

London Health Sciences Centre - University Hospital

London, Ontario, Canada

Victoria Hospital

London, Ontario, Canada

Outcomes

Primary Outcomes

Adverse events (patient) - Decrease in oxygenation

Count of any decreases in oxygenation, expressed as PaO2 (mmHg) / FiO2 (% oxygen as a decimal), of greater than 20% during the BLES treatment and up to 30 minutes post-treatment. Change will be calculated relative to pre-treatment values.

Time frame: 3 days post-randomization

Adverse events (patient) - Decrease in hemodynamics

Count of any decrease in mean arterial blood pressure \>10 mmHg or requirement for \>20% increase in vasopressor dose during the BLES procedure and up to 30 minutes post-treatment. Change will be calculated relative to the pre-treatment values.

Time frame: 3 days post-randomization

Adverse event (healthcare worker) - Circuit breach

Number of circuit breaches. Count of any circuit breach immediately prior to and during each BLES treatment procedure will be recorded.

Time frame: 3 days post-randomization

Adverse event (healthcare worker) - COVID-19 symptoms

Count of healthcare personnel involved in the BLES procedure developing symptoms and testing positive for COVID-19.

Time frame: 2 weeks post-randomization

Secondary Outcomes

Change in oxygenation

PaO2 (in mmHg) / FiO2 (percentage oxygen expressed as a decimal) ratios captured from clinical chart

Time frame: Every 12 hours post-randomization until ICU discharge or death, whichever comes first, an average of 10 days and assessed up to 30 days.

Change in Lung compliance

Lung compliance captured from the ventilators, expressed in mL/cm H2O.

Time frame: Every 12 hours post-randomization until ICU discharge or death, whichever comes first, an average of 10 days and assessed up to 30 days.

Data from ClinicalTrials.gov

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