Nebulised Rt-PA for ARDS Due to COVID-19

PHASE2CompletedINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

April 22, 2020

Primary Completion Date

March 18, 2021

Study Completion Date

March 18, 2021

Conditions
COVID
Interventions
DRUG

Nebulised recombinant tissue-Plasminogen Activator (rt-PA) - Cohort 1

"Patients in the rt-PA group received the first dose as soon as possible after registration.~Initial dosing regime: 10 mg of rt-PA dissolved in 5 ml of diluent given every 6 hrs (resulting in a total daily dose of 40mg) for a maximum of 66 hrs, in addition to standard of care for COVID-19 acute respiratory distress syndrome (ARDS). Following protocol amendment, dosing duration was increased from 3 days to up to 14 days of rt-PA treatment."

DRUG

Nebulised recombinant tissue-Plasminogen Activator (rt-PA) - Cohort 2 IMV

Patients on IMV received 60mg daily over three doses for up to 14 days

DRUG

Nebulised recombinant tissue-Plasminogen Activator (rt-PA) - Cohort 2 NIV

NIV patients received 60mg daily over 3 doses for two days, followed by 12 days receiving 40mg daily over two doses.

Trial Locations (1)

NW3 2QG

The Royal Free Hospital, London

All Listed Sponsors
lead

University College, London

OTHER

NCT04356833 - Nebulised Rt-PA for ARDS Due to COVID-19 | Biotech Hunter | Biotech Hunter