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Neurologic Physiology After Removal of Therapy (NeuPaRT)

Neurologic Physiology After Removal of Therapy (NeuPaRT): Pilot Multicentre Feasibility Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05306327
Acronym
NeuPaRT
Enrollment
158
Registered
2022-04-01
Start date
2022-10-18
Completion date
2027-03-01
Last updated
2026-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Determination of Death

Brief summary

The purpose of this study is to determine when brain function stops compared to when the heart stops by monitoring electrical brain activity in patients who are taken off life support and progress to death in the intensive care unit.

Detailed description

There are many Canadians who need an organ transplant and who will never get one. In the past, people could only be organ donors after being declared brain dead. The dead donor rule serves this purpose by ensuring that death determination precedes organ retrieval. In Canada, death determination occurs in one of two ways. In neurologic determination of death (NDD), death is declared upon completion of a standardized neurologic assessment that confirms permanent loss of brain activity. In donation after circulatory determination of death (DCDD), death is declared 5 minutes after circulatory arrest. By confirming permanent loss of brain activity, the current NDD process protects donors from suffering and maintains stakeholder trust. In contrast, the current DCDD process assumes, but does not explicitly confirm, permanent loss of brain activity when death is declared 5 minutes after circulatory arrest. While this assumption is rooted in a strong physiologic rationale, lack of compelling evidence regarding cessation of brain activity in humans contributes to ongoing mistrust of the DCDD process among healthcare and public stakeholders.

Interventions

DIAGNOSTIC_TESTelectroencephalography (EEG)

1. brain cortical activity using full scalp 2. cerebral blood flow velocity 3. during the dying process following planned withdrawal of life sustaining measures (WLSM)

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years 2. Plan for the withdrawal of life sustaining measures (WLSM) 3. Attending physician anticipates patient will die within 24 hours of the withdrawal of life sustaining measures 4. Patient has an indwelling arterial cannula for monitoring blood pressure

Exclusion criteria

1. Brain death or plan for Neurologic Determination of Death (NDD) 2. Injuries that anatomically preclude the use of neurologic monitoring

Design outcomes

Primary

MeasureTime frameDescription
Patient Accrual complete study procedures)2022 to 202390 patients at all sites and an additional 18 patients at the lead site for specific tests

Secondary

MeasureTime frameDescription
Waveform Data Completeness2022-2023Adequate waveform signal that (i) spans circulatory arrest, (ii) includes data for at least 80% of the planned observation period (from the withdrawal of life sustaining measures to 30 minutes after circulatory arrest \[or 5 minutes for confirmed donation after circulatory determination of death (DCDD) donors\]), and (iii) has a clearly identifiable time of cessation for each signal.
Time Difference Circulatory Arrest and Cessation of EEG Activity2022-2023Cerebral blood flow velocity in middle cerebral artery (when available), and cessation of event/evoked potentials (LHSC site only). See below for definition of cessation of each signal.

Countries

Canada

Contacts

CONTACTTeneille Gofton
teneille.gofton@lhsc.on.ca519-663-2911
CONTACTMarat Slessarev
marat.slessarev@lhsc.on.ca519-685-8500
PRINCIPAL_INVESTIGATORTeneille Gofton, MD MSc FRCPC

London Health Sciences Centre

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026