Advanced Respiratory Monitoring for Safer Mechanical Ventilation in Patients Without Respiratory Failure
Recruiting
Observational Study
Developing Acute Respiratory Distress Syndrome
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 40 (estimated)
- Sponsor
- Istituto Clinico Humanitas · Other
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About This Trial
Patients admitted to the intensive care unit (ICU) and mechanically ventilated for reasons other than acute respiratory failure, such as coma, trauma, or sepsis, are at risk of developing acute respiratory distress syndrome (ARDS), which increases the duration of mechanical ventilation, mortality, and functional dependence at discharge.
Trial Locations
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Eligibility 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…
Contacts
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