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Prone Positioning for Brain-injured Patients With Severe ARDS (ProBrain)

Prone Positioning for Brain-injured Patients With Severe ARDS (ProBrain)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05050838
Acronym
ProBrain
Enrollment
11
Registered
2021-09-21
Start date
2018-08-01
Completion date
2020-06-30
Last updated
2021-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Blood Flow

Keywords

Prone Position, Acute Respiratory Distress Syndrome, Intracranial Pressure

Brief summary

Prone position (PP) is a key component to treat hypoxemia in patients with severe acute respiratory distress syndrome (ARDS). However, most studies evaluating PP effects in patients with ARDS exclude those with brain-injuries without providing any medical evidence. This prospectice observational study aimed to investigate if prone positioning leads to significant modification of cerebral perfusion in brain-injured patients with ARDS.

Interventions

TCD ultrasonography is based on the principle of the Doppler effect. According to this principle, ultrasound waves emitted from the Doppler probe are transmitted through the skull and reflected by moving red blood cells within the intracerebral vessels. The difference in the frequency between the emitted and reflected waves, referred to as the Doppler shift frequency, is directly proportional to the speed of the moving red blood cells (blood flow). Cerebral blood flow (in cm/s) of the middle cerebral artery will be measured with TCD in blood-injured ARDS patients before and one hour after prone positioning (normal ranges: 48 to 72 cm/s).

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Age
18 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* adult's patients suffering from brain injuries * patients neurologically monitored with TCD * patients requiring prone position for severe ARDS

Exclusion criteria

* pregnant women * patients with contrindication to prone position

Design outcomes

Primary

MeasureTime frameDescription
Cerebral Blood Flow1 hourCerebral Blood Flow measurement before and after prone positioning

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026