Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05679739

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

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
49 (estimated)
Sponsor
National University Hospital, Singapore · Academic / Other
Sex
All
Age
21 Years – 79 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHERIndividualized blood pressure strategyAn individualized blood pressure strategy targeting cerebral blood flow, serially guided by near-infrared spectroscopy and transcranial Doppler ultrasound. Assessments are performed on admission, and at 12, 24 and 48 hours post-ROSC.

Timeline

Start date
2023-08-29
Primary completion
2025-08-01
Completion
2026-08-01
First posted
2023-01-11
Last updated
2025-05-16

Locations

1 site across 1 country: Singapore

Source: ClinicalTrials.gov record NCT05679739. Inclusion in this directory is not an endorsement.