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Investigating the Localization of Consciousness Through Patients with Disorders of Consciousness: Anterior Vs. Posterior Cortex Debate

H

Hangzhou Normal University

Status

Completed

Conditions

Disorders of Consciousness

Study type

Observational

Funder types

Other

Identifiers

NCT06770348
20230630

Details and patient eligibility

About

Patients enrolled in the study underwent five assessments using the CRS-R(Coma Recovery Scale-Revised) within 10 days, along with an 18F-FDG-PET scan.

Full description

Patients enrolled in the study underwent five assessments using the CRS-R (Coma Recovery Scale-Revised) within 10 days, along with an 18F-FDG-PET (18F-fluorodeoxyglucose-positron emission tomography) scan. The CRS-R evaluations were conducted by professionally trained and highly experienced personnel. During the CRS-R assessments, patients' behavioral responses were recorded in the domains of visual, auditory, motor, oromotor/verbal, communication, and arousal. Based on the optimal CRS-R results obtained within the 10-day period, patients were categorized into MCS (Minimally consciousness state, criteria: consistent command-following, reproducible responses to commands, object recognition, intelligible verbalization, partially accurate communication, object localization, visual pursuit and visual object localization, spontaneous motor responses, object manipulation, and/or localization to noxious stimulation) or UWS (Unresponsive wakefulness syndrome, criteria: preserved wakefulness accompanied by behavioral responses such as localization to sound, auditory startle, visual startle, withdrawal/flexion movements, abnormal posturing, vocalizations/oromotor movements, and reflexive oromotor responses). All patients exhibited stable vital signs. For data analysis, a healthy control group from Belgium was included to compare brain metabolism between patients with disorders of consciousness and healthy individuals.

Enrollment

100 patients

Sex

All

Ages

18 to 81 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Confirmed diagnosis of disorders of consciousness after 5 CRS-R assessments;
  • Age >18 years;
  • Stable vital signs;
  • No use of sedatives or neuromuscular blockers within 24 hours prior to enrollment.

Exclusion criteria

  • Acute-phase patients (injury duration <28 days);
  • Fewer than 5 CRS-R assessments completed within 10 days;
  • Patients diagnosed with EMCS (Emerging Minimally Conscious State);
  • Patients with unclear diagnoses (cases where experienced evaluators could not reach a consensus diagnosis);
  • Patients with persistent seizures.

Trial design

100 participants in 3 patient groups

UWS (Unresponsive Wakefulness Syndrome)
Description:
presence of basic arousal, localization to sound, auditory startle responses, visual startle responses, flexion withdrawal, abnormal posturing, vocalization/oromotor responses, and/or reflexive oromotor movements.
MCS (Minimally Conscious State)
Description:
based on the following criteria: stable responses to commands, the ability to repeat commands, object recognition, understandable speech, incomplete communication, object localization, visual tracking, visual object localization, voluntary motor responses, manipulation of objects, and/or localization of noxious stimuli.
HC (Healthy control)
Description:
people with full consciousness

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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