Actively Recruiting

Age: 18Years +
All Genders
NCT07269743

AEROSOL THERAPY IN ARDS PATIENTS (AERO-IN-ARDS)

Led by TS Misra Medical College · Updated on 2025-12-15

423

Participants Needed

1

Research Sites

55 weeks

Total Duration

On this page

Sponsors

T

TS Misra Medical College

Lead Sponsor

A

All India Institute of Medical Sciences

Collaborating Sponsor

AI-Summary

What this Trial Is About

Aerosol therapy delivers medicines as a fine mist directly into the lungs. This allows faster action and fewer whole-body side effects. It is a key treatment for diseases such as asthma and COPD. In acute respiratory distress syndrome (ARDS), early laboratory and small clinical studies suggested that inhaled beta-2 agonists and corticosteroids might help the lungs heal by improving mucus clearance, reducing inflammation, and helping remove excess fluid. However, larger randomized trials have not shown clear clinical benefits. Therefore, major guidelines do not provide specific recommendations for aerosol use in ARDS. There are also safety concerns, including risks of low potassium levels, abnormal heart rhythms, worsening lung function, and increased healthcare costs. Despite these uncertainties, our previous study showed that aerosol therapy continues to be used widely in ARDS patients. However, that study was small and limited to one country, so the findings may not apply to other regions. To address this gap, we have designed Aero-in-ARDS, a large, multi-national, prospective observational study. This study will investigate how often aerosol therapy is used in ARDS, what types of aerosol drugs are given, and how practices differ across countries. By identifying current patterns and comparing them with existing evidence, the study aims to highlight gaps in knowledge and guide future research.

CONDITIONS

Official Title

AEROSOL THERAPY IN ARDS PATIENTS (AERO-IN-ARDS)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients newly admitted to participating ICUs with a diagnosis of ARDS
  • Patients requiring mechanical ventilation
  • Age 18 years or older
  • Informed consent obtained if required by local regulations
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Patients managed with non-invasive ventilation (NIV) or high-flow nasal oxygen (HFNO)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ts Misra Medical College

Lucknow, Uttar Pradesh, India, 226008

Actively Recruiting

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Research Team

P

Piyush srivastava, MD

CONTACT

S

Sanjay Singhal, MD, EDRM, FCCP, PGDAST

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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