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Study identifier: NCT04459806 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Intracranial PrEssure Time dOse (ImPETO)

Condition: Intracranial Hypertension · Traumatic Brain Injury · Subarachnoid Hemorrhage  ·  Sponsor: University of Milano Bicocca

PhaseN/A
Planned participants250
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The new Integra CereLink ICP monitor integrate the possibility of recording and displaying continuously the AUC (Pressure Time Dose, PTD) and other ICP derived variables and provide the possibility of evaluating the utility of this information at the bedside. It offers the opportunity to test in a standardized way the clinical value of the PTD computation in this setting. Therefore, this study aims to test clinically if PTD recorded continuously is associated to patients' outcome and to identify a threshold of PTD associated with the transition from good to negative outcomes.

This description comes directly from the study's public registry record.

Talk to the study team

Giuseppe Citerio, Professor  ·  +39039233  ·  giuseppe.citerio@unimib.it

Always discuss trial participation with your own doctor first.

Locations (1)

Fondazione IRCCS San Gerardo dei TintoriMonza, MB, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT04459806