Clin2
NCT05075161Possibly a fitRecruiting

Pirfenidone to help prevent lung scarring in ARDS

Acute Respiratory Distress Syndrome (ARDS)

Treatments studied

Part of Lungs & breathing clinical trials.

This Phase 3 trial tests whether pirfenidone can prevent or reduce lung scarring (fibrosis) in adults with ARDS who are within about a week of their illness starting. It may help by lowering harmful inflammation and the body’s scarring response.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
130 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You’re 18 years or older
  • You have ARDS that started within 1 week of a known event or new/worsening breathing symptoms
  • Chest X-ray shows problems in both lungs that aren’t fully explained by fluid buildup, collapsed lung, or lung nodules
  • Your breathing is significantly impaired (oxygen levels with ventilation support meet the study cutoff)
  • You fit an “inflammatory ARDS” pattern (at least one: high inflammation blood tests, needing medicines to support blood pressure, or certain blood chemistry signals like low bicarbonate or high lactate)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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