Study on Aspirin’s Role in Reducing COVID-19 Risk for Patients with Aspirin-Exacerbated Respiratory Disease

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What is this study about?

This clinical trial is focused on studying a condition known as aspirin-exacerbated respiratory disease (AERD). AERD is a respiratory condition that can worsen with the use of aspirin. The study is investigating whether long-term use of aspirin, specifically a 300 mg tablet form known as ACARD, can reduce the risk of infection with the SARS-CoV-2 virus, which causes COVID-19, in patients with AERD.

The purpose of the study is to see if aspirin, which works by blocking a specific enzyme in the body, can help predict a lower chance of getting infected with the virus. The study will also look at certain genetic features that might influence how the body responds to the virus when taking high doses of aspirin. Participants will be given either aspirin or a placebo, which is a substance with no active medication, to compare the effects.

Throughout the study, researchers will monitor changes in specific genes that might be linked to a reduced risk of SARS-CoV-2 infection. The study will last for a period of time, during which participants will take the medication and have regular check-ups to assess their health and any changes in their condition. The goal is to better understand how aspirin might help in managing the risk of COVID-19 in people with AERD.

1 joining the study

Upon joining the study, you will be required to sign an informed consent form. This document confirms your understanding of the study and your agreement to participate.

You must be between 18 and 70 years old and meet specific health criteria. For patients with aspirin-exacerbated respiratory disease (AERD), your lung function must be at least 70% of the predicted value. If you are a healthy control participant, you must not have asthma.

2 medication administration

You will be given a medication called ACARD 300 mg, which contains acetylsalicylic acid. This is commonly known as aspirin.

The medication is in the form of a tablet and is taken orally. The dosage and frequency will be determined by the study team based on your specific needs and health status.

3 monitoring and assessments

Throughout the study, your health will be closely monitored. This includes regular assessments of your lung function and other health parameters.

You may be asked to provide samples, such as sputum or nasal cells, to help assess the effects of the medication on your body.

4 study duration

The study is expected to continue until February 28, 2025. Your participation may last for the entire duration or a portion of it, depending on your health and the study’s requirements.

Regular follow-ups will be scheduled to ensure your safety and to gather necessary data for the study.

Who Can Join the Study?

  • Must sign an informed consent form, which means you agree to participate after understanding the study.
  • Must be between 18 and 70 years old.
  • For patients with aspirin-exacerbated respiratory disease (AERD):
    • Must have a baseline FEV1 of at least 70% of the predicted value. FEV1 is a measure of how much air you can forcefully exhale in one second, and it helps assess lung function.
    • Must not be pregnant, and if you are of childbearing potential, you must use highly effective contraception.
  • For healthy control participants:
    • Must be in healthy condition.
    • Must not have asthma.

Who Cannot Join the Study?

  • Patients who do not have aspirin-exacerbated respiratory disease cannot participate. This is a condition where taking aspirin can worsen breathing problems.
  • Patients who are not within the specified age range cannot participate. The study is open to certain age groups only.
  • Patients who are part of a vulnerable population cannot participate. This means people who might need special protection or care.

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

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Other Sites

Site Name City Country Status
Samodzielny Publiczny Zaklad Opieki Zdrowotnej Szpital Uniwersytecki W Krakowie Cracow Poland

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Poland Poland
Not recruiting
31.01.2023

Trial locations

Investigated drugs:

Aspirin is a medication commonly used to relieve pain, reduce inflammation, and lower fever. In this clinical trial, aspirin is being studied to see if it can help reduce the risk of getting infected with the virus that causes COVID-19, especially in people who have a condition called aspirin-exacerbated respiratory disease (AERD). This condition makes it hard for some people to breathe when they take aspirin, but the study is looking at whether taking aspirin regularly might actually help protect against the virus. The trial is also exploring if certain genetic traits in people might make aspirin more or less effective in preventing the infection.

Aspirin-Exacerbated Respiratory Disease – Aspirin-Exacerbated Respiratory Disease (AERD) is a chronic medical condition characterized by asthma, nasal polyps, and sensitivity to aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs). The disease progresses with respiratory symptoms such as wheezing, coughing, and shortness of breath, often triggered by aspirin or NSAID intake. Over time, individuals with AERD may experience worsening asthma symptoms and recurrent nasal polyps, which can lead to nasal congestion and loss of smell. The condition is associated with an overproduction of leukotrienes, inflammatory chemicals in the body. AERD can also lead to chronic sinusitis, a persistent inflammation of the sinuses. The progression of symptoms can vary among individuals, with some experiencing more severe respiratory issues than others.

Trial ID:
2024-514602-31-00
Protocol code:
AERD-COV19
Trial Phase:
Therapeutic use (Phase IV)

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