Study of Chronic Antihistamine and Amantadine Treatments in COVID-19 Outcomes
Led by Consorci Sanitari de Terrassa · Updated on 2026-04-03
140660
Participants Needed
2
Research Sites
161 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating how chronic treatment with antihistamines or amantadine might affect the course of COVID-19 infection. The study aims to measure rates of symptomatic COVID-19 infection, hospital admissions, survival, post-COVID syndrome, and thrombosis in patients receiving these treatments. Data will be compared with age-matched groups from the general population in the Terrassa Health Consortium.
The study observes patients already taking antihistamines or amantadine as a chronic treatment, tracking their health outcomes related to COVID-19 from March 2020 onward. Comparisons will be made between these patients and others within the same age groups from the general population. No new treatments are given this is an observational study assessing existing medication use.
Participants are monitored for hospital admissions, survival, symptomatic infection, and complications like post-COVID syndrome and thrombosis. The study uses health records to collect this data and compares outcomes between the treatment group and general population over time. The total study period covers from March 2020 to February 2028, with ongoing data collection and analysis.
CONDITIONS
Brief Title
Antihistamines, Amantadine and Evolution of COVID-19
Research Team
A
Anna Puigdellivol, Ph.D
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Patients having chronic treatment with antihistamines or amantadine
You will not qualify if you...
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote) to confirm chronic treatment and health status
Long-term Monitoring
Duration - From March 2020 through January 2025
Participants who have chronic treatment with antihistamines or amantadine are observed to evaluate the rate of COVID-19 infection, hospitalization, survival, post-COVID syndrome, and thrombosis.
Periodic assessments depending on health status and routine care
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Study of Chronic Antihistamine and Amantadine Treatments in COVID-19 Outcomes