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Study identifier: NCT05679739 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

NEUROprotection Via optimizINg Cerebral Blood Flow afTer cArdiaC arresT (NEURO-INTACT) Study

Condition: Out-Of-Hospital Cardiac Arrest (OHCA)  ·  Sponsor: National University Hospital, Singapore

PhaseNA
Planned participants49
Who can joinAll sexes, 21 Years to 79 Years
Healthy volunteersNo

About this study

This single-center proof of concept study aims to assess the efficacy of a blood pressure strategy targeting person- and time-specific cerebral blood flow compared with standard-of-care using neuron-specific enolase as a quantitative biomarker of brain injury. Our central hypothesis is that an individualized blood pressure strategy targeting cerebral perfusion will reduce the extent of brain injury as indicated by changes in levels of neuron-specific enolase from baseline at 72 hours. To test this hypothesis, we will recruit 49 patients to an individualized blood pressure management strategy targeting cerebral blood flow, where optimal blood pressure will be serially calculated by the ICM+ brain monitoring software (Cambridge, UK) using inputs from transcranial Doppler ultrasound and near-infrared spectroscopy.

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

Talk to the study team

Shir Lynn Lim  ·  69082222  ·  shir_lynn_lim@nuhs.edu.sg

Always discuss trial participation with your own doctor first.

Locations (1)

National University Heart Centre, SingaporeSingapore, SingaporeRecruiting

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Source record: clinicaltrials.gov/study/NCT05679739