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Camostat MesylateWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (4)


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

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D020141 Hemostatic Disorders NIH 0.30
D001778 Blood Coagulation Disorders NIH 0.30

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0001928 Abnormality of coagulation HPO 0.30

There is one clinical trial.

Clinical Trials


1 The Utility of Camostat Mesylate in Patients With COVID-19 Associated Coagulopathy (CAC) and Cardiovascular Complications

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.

NCT04435015 Coagulopathy Cardiovascular Complication COVID-19 Drug: Camostat Mesylate Drug: Microcrystalline Cellulose, NF
MeSH:Hemostatic Disorders Blood Coagulation Disorders
HPO:Abnormality of coagulation Abnormality of the coagulation cascade

Primary Outcomes

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 days

Secondary Outcomes

Description: 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 months

Description: Percent change in fibrinogen over 7 days compared to day 1

Measure: Change in plasma Fibrinogen levels

Time: 7 days

Description: Percent change in troponin over 7 days compared to day 1

Measure: Change in plasma troponin

Time: 7 days

Description: 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 days

Description: Days with hypoxia (Room Air O2 Sat<93%) or days intubated

Measure: Duration of intubation

Time: 7 days

Description: The number of days in the intensive care unit

Measure: Length of stay in the intensive care unit

Time: 28 days

Description: The number of days since admission to discharge

Measure: Time to discharge from hospital

Time: 30 days

Description: 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


Related HPO nodes (Using clinical trials)