Name (Synonyms) | Correlation | |
---|---|---|
drug1005 | Graded exercise test Wiki | 1.00 |
drug590 | Cloth Face Mask Wiki | 1.00 |
drug1539 | N-95 Respirator Wiki | 1.00 |
drug1488 | Microcrystalline Cellulose, NF Wiki | 1.00 |
There is one clinical trial.
The primary aim of this study is to determine whether Camostat mesylate reduces SARS-COV-2 associated coagulopathy. Additional aims are to determine the effect of Camostat mesylate on SARS-COV-2 associated myocardial injury, to assess duration of hypoxia or intubation, to evaluate the length of intensive care unit and hospital stay, and assess mortality rates.
Description: The sum percent change in D-Dimer over 7 days will be compared to day 1
Measure: Percent change in plasma D-Dimer Time: 7 daysDescription: The first assessment on mortality and complications will be carried out 3 months after the start of the study.
Measure: Overall Safety and adverse event Time: 3 monthsDescription: Percent change in fibrinogen over 7 days compared to day 1
Measure: Change in plasma Fibrinogen levels Time: 7 daysDescription: Percent change in troponin over 7 days compared to day 1
Measure: Change in plasma troponin Time: 7 daysDescription: New onset cardiomyopathy defined by a reduction of EF by greater than 10% or less than 45% will be measured
Measure: New onset cardiomyopathy Time: 7 daysDescription: Days with hypoxia (Room Air O2 Sat<93%) or days intubated
Measure: Duration of intubation Time: 7 daysDescription: The number of days in the intensive care unit
Measure: Length of stay in the intensive care unit Time: 28 daysDescription: The number of days since admission to discharge
Measure: Time to discharge from hospital Time: 30 daysDescription: The ocurrence of major adverse cardiovascular events (MACE): MI, stroke, CHF, PCI, death from cardiovascular disease will be studied.
Measure: Occurrence of major adverse cardiovascular events Time: 7 days