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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Maximum Age: 79
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
Singapore
National University Heart Centre, Singapore
RECRUITING
Singapore
Contact Information
Primary
Shir Lynn Lim
shir_lynn_lim@nuhs.edu.sg
69082222
Time Frame
Start Date: 2023-08-29
Estimated Completion Date: 2026-08
Participants
Target number of participants: 49
Treatments
Experimental: Individualized blood pressure strategy
Hemodynamic optimization performed to an individualized target mean arterial pressure in the first 72 hours post ROSC based on cerebral perfusion assessed serially.
Related Therapeutic Areas
Sponsors
Leads: National University Hospital, Singapore

This content was sourced from clinicaltrials.gov