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Impact of Respiratory Virus in Critically Ill Patients With Acute Respiratory Failure

Impact of Respiratory Virus in Critically Ill Patients With Acute Respiratory Failure

Recruiting
19 years and older
All
Phase N/A

Overview

This is an observational study to evaluate the clinical impact of respiratory virus in the patients with acute respiratory failure

Eligibility

Inclusion Criteria:

  • Male or female aged 19 years
  • Written informed consent by the patient or legally authorized representative
  • Critical illness consistent with acute respiratory failure, to be enrolled within 24 hours of presentation

Exclusion Criteria:

  • No informed consent
  • A patient who is judged to be unable to make a voluntary decision by understanding information about this research due to cognitive vulnerability

Study details
    Pulmonary Disease
    ADULT RESPIRATORY DISTRESS SYNDROME
    Acute Respiratory Failure

NCT04411368

Seoul St. Mary's Hospital

16 February 2024

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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