Corona Virus Disease 19 (Covid 19) Clinical Trial
— GRECCO-19Official title:
The GReek Study in the Effects of Colchicine in Covid-19 cOmplications Prevention
Verified date | April 2021 |
Source | National and Kapodistrian University of Athens |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Based on data regarding the effect of colchicine on the inflammasome NLP3 and microtubule formation and associations thereof with the pathogenetic cycle of SARS-COV-2, the question arises whether colchicine, administered in a relatively low dose, could potentially have an effect the patients' clinical course by limiting the myocardial necrosis and pneumonia development in the context of COVID-19. If present, this effect would be attributed to its potential to inhibit inflammasome and (less probably) to the process of SARS-CoV-2 endocytosis in myocardial and endothelial respiratory cells.
Status | Terminated |
Enrollment | 105 |
Est. completion date | April 27, 2020 |
Est. primary completion date | April 27, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: Patients >18 years old with laboratory confirmed SARS-CoV-2 infection (RT PCR) AND body temperature >37.5 degrees centigrade AND at least two of: i. sustained coughing, ii. sustained throat pain, iii. anosmia and/or ageusia, iv. fatigue/tiredness, v. PaO2<95 mmHg. Exclusion Criteria: - pregnancy, lactation; - known hypersensitivity to colchicine - known hepatic failure - eGFR<20 ml/min - clinical estimation that the patient will require mechanical respiratory support in less than 24 hours - any clinical estimation of the attending physician under which the patient shall be excluded - QTc > 450 msec (colchicine is not known to significantly prolong QTc, but may interact with other medications which prolong QTc). - participation in another clinical trial - under colchicine treatment for other indications - patient who is not likely to comply to study procedures |
Country | Name | City | State |
---|---|---|---|
Greece | National and Kapodistrian University of Athens | Athens |
Lead Sponsor | Collaborator |
---|---|
National and Kapodistrian University of Athens |
Greece,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Clinical deterioration in the semiquantitative ordinal scale suggested by the WHO R&D committee | Time to clinical deterioration (2 levels in the WHO R&D Blueprint scale) | 3 weeks | |
Primary | Maximal concentration of cardiac troponin | Maximal concentration of high-sensitivity cardiac troponin | 10 days |