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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-79
SponsorNational University Hospital, Singapore

About this trial

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.

Eligibility criteria

Qualifiers

At least 21 years of age

Comatose defined as not being able to obey verbal commands and no verbal response to pain after sustained ROSC.

Disqualifiers

≥ 80 years old at time of enrolment

Pregnant patients

Limitations of care or life support therapy withdrawn within 24 hours of admission

Trial design

Treatments tested in this trial

  • Individualized blood pressure strategy

Treatment groups

49 Participants
are divided into 1 treatment group