About this trial
The rates of symptomatic COVID19 infection, hospital admission among COVID19 cases and survival would be quantified in patiens chronically treated with antihistamines or amantadine, with the aim of determining the role of antihistamines and amantadine in the evolution of COVID19.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
Population assigned to the Public and free Access Terrassa Health Consortium
Trial design
Case-control
Retrospective
Treatments tested in this trial
Antihistamine
DrugObservation of the rate of COVID19 infection, the rate of hospitalization, the rate of survival and postcovid syndrome and thrombosis among patients previously treated with antihistamines
Amantadine
DrugObservation of the rate of COVID19 infection, the rate of hospitalization, the rate of survival and the rate of postcovid syndrome and thrombosis among patients previously treated with amantadine
Treatment groups
Trial outcomes
Primary outcomes
Hospital Admissions.
Rate of Hospitalization among COVID 19 infections
Secondary outcomes
Survival
Survival among COVID1 hospitalized cases.
Symptomatic infection
Patients suffering a symptomatic COVID19 infection within a determinate age group
Postcovid syndrome
Patients developing postcovid syndrome after COVID19 infection
Thrombosis
Patients developing thrombosis (with particular assessment of stroke, cardiac infarction, retinal vessels and pulmonary embolism)
Sponsors and contacts
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Consorci Sanitari de Terrassa
Lead sponsor
Institut Català de la Salut
Collaborator