Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Lung and brain ultrasound to guide PEEP in adults with ARDS and acute brain injury

Official title: The Contribution of the Combination of Transthoracic and Transcranial Ultrasonography to the Titration of Positive End-expiratory Pressure in Patients With Acute Respiratory Distress Syndrome and Acute Brain Injury

Run by George Papanicolaou Hospital · NCT07248995 · Data updated 2026-11-12

This trial will test whether combining lung and transcranial ultrasound helps doctors choose the best PEEP level for adults on a ventilator with ARDS and acute brain injury.

More Acute Respiratory Distress Syndrome (ARDS) trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorGeorge Papanicolaou Hospital
Academic / other
Locations1 site (Thessaloniki)
StatusRecruiting
StartedDecember 1, 2025
Main results expectedMay 2027
Study endsJuly 2027
Registry record updatedDecember 31, 2025
Trial IDNCT07248995 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18) with severe acute brain injury and ARDS within the first 10 days of ICU admission who are mechanically ventilated, have invasive neuromonitoring, and acceptable ultrasound acoustic windows are ideal candidates.

Probably not a fit

Patients with severe chronic brain or pulmonary disease, brain tumor or CNS infection, decompressive craniectomy, severe coagulopathy, poor acoustic windows, or those without invasive neuromonitoring are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study uses a stepwise PEEP increase protocol in mechanically ventilated adults who have ARDS and acute brain injury. Lung ultrasound will provide a Lung Ultrasound Score to track aeration and guide recruitment maneuvers, while transcranial Doppler will monitor cerebral blood flow surrogates such as the pulsatility index to detect adverse cerebral responses. Investigators will integrate both imaging assessments to select a PEEP level that improves lung function without compromising cerebral hemodynamics. The overarching aim is to develop an individualized, brain-protective ventilation strategy for this high-risk population.

Why it matters

Potential benefit: If successful, this approach could identify safer PEEP settings that improve oxygenation while minimizing increases in intracranial pressure, potentially reducing respiratory and neurological complications.

How similar studies have gone: Lung ultrasound and transcranial Doppler have been used separately to guide ventilation and monitor cerebral hemodynamics, but combining them to titrate PEEP in ARDS with acute brain injury is relatively novel and has limited prior evidence.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥ 18 years
* Severe acute brain injury (e.g., traumatic brain injury, subarachnoid hemorrhage, intracerebral hemorrhage, acute ischemic stroke)
* Development of ARDS (according to Berlin criteria) within the first 10 days of ICU admission

Exclusion Criteria:

* Severe chronic brain diseases
* Brain tumor or central nervous system (CNS) infection
* Severe chronic pulmonary or cardiovascular disease
* Severe coagulopathy
* Undergoing decompressive craniectomy
* Lack of invasive neuromonitoring
* Withdrawal of life-sustaining treatment
* Poor acoustic window in ultrasound

Where it's running

  • George Papanikolaou General Hospital
    Thessaloniki, Greece
    Recruiting

Study contacts

  • Principal investigator: Theodoros Schizodimos, MD — 2nd Intensive Care Unit, George Papanikolaou General Hospital of Thessaloniki
  • Study coordinator: Theodoros Schizodimos, MD
  • Email: teoschizo@gmail.com
  • Phone: +306973439717

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.