Evaluating the effects of antihistamines and amantadine on COVID-19 outcomes

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to quantify the rates of symptomatic COVID-19 infection, hospital admissions, and survival among patients who are chronically treated with antihistamines or amantadine. The research will analyze data from patients in nursing homes and compare their outcomes with a control group from the Terrassa Health Consortium. By stratifying results by age groups, the study seeks to determine the potential protective roles of these medications in the evolution of COVID-19.

Why it matters

Who can join: the full rules

Inclusion Criteria: Patients having chronic treatment with antihistamines or amantadine -

Exclusion Criteria: None

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Where it's running

• Hospital de Terrassa
  Terrassa, Barcelona, Spain Recruiting
• Hospital of Terrassa
  Terrassa, Barcelona, Spain Recruiting

Study contacts

• Principal investigator: Anna Puigdellívol, PhD — Terrassa Health Consortium
• Study coordinator: Anna Puigdellivol, Ph.D
• Email: apuigdellivol@cst.cat
• Phone: 34-93-5884555

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.