Clinical trial Recruiting at 1 site Observational Ages 18 and up

Advanced respiratory monitoring to help safer ventilation in ICU patients without respiratory failure

Official title: Advanced Respiratory Monitoring for Safer Mechanical Ventilation in Patients Without Respiratory Failure

Run by Istituto Clinico Humanitas · NCT07686315 · Data updated 2026-11-12

This study tests whether using advanced respiratory monitoring in adults who are intubated for reasons other than respiratory failure can help prevent ARDS.

More Acute Respiratory Distress Syndrome trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment40 (estimated)
SponsorIstituto Clinico Humanitas
Academic / other
Locations1 site (Milan, Lombardy)
StatusRecruiting
StartedJune 30, 2026
Main results expectedDecember 30, 2026
Study endsDecember 30, 2026
Registry record updatedJuly 7, 2026
Trial IDNCT07686315 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older who are invasively ventilated for non-respiratory reasons (e.g., coma, trauma, sepsis) and begin monitoring within 24 hours of intubation at a participating center.

Probably not a fit

Patients who do not develop ARDS or who do not experience changes in ventilation strategy based on monitoring may see no direct benefit.

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 will enroll adults 18 and older who are invasively ventilated for conditions such as coma, trauma, or sepsis. Monitoring includes continuous airway and esophageal pressure, flow measurements, and lung ventilation distribution to tailor ventilation settings. The goal is to see if applying these monitoring techniques in patients without initial respiratory failure can reduce the risk of developing ARDS and related complications. Data from this single-site initiative at Humanitas Research Hospital will help determine feasibility and potential impact on ventilator strategy. The study does not assign a treatment but observes outcomes associated with enhanced monitoring practices.

Why it matters

Potential benefit: If successful, enhanced monitoring could help clinicians personalize ventilation to reduce ARDS risk and improve outcomes for ICU patients on mechanical ventilation.

How similar studies have gone: Prior use of advanced respiratory monitoring in ARDS has shown benefits; applying these techniques in non-respiratory failure patients is investigational with limited prior evidence.

Who can join: the full rules

Show full inclusion / exclusion criteria
Study Population Eligibility Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No

Inclusion Criteria:

Adult patients +18 years. Undergoing invasive mechanical ventilation for reasons other than acute respiratory failure (such as coma, trauma, or sepsis).

Initiation of monitoring within 24 hours of oro-tracheal intubation.

Exclusion Criteria:

Evidence of pneumothorax, pneumomediastinum, or subcutaneous emphysema. Pregnancy. Absolute contraindications to nasogastric tube placement. Absolute contraindications to electrical impedance tomography (EIT) monitoring.

Where it's running

  • Humanitas Research Hospital
    Milan, Lombardy, Italy
    Recruiting

Similar studies

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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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.