ClinicalTrials.Veeva

Menu

Aiming for a Better Understanding and Improvement of the Diagnosis and Prognosis of Patients With Disorders of Consciousness Through Multimodal Observations (PerBrain)

P

Paris Brain Institute (ICM)

Status

Unknown

Conditions

Unresponsive Wakefulness Syndrome
Minimally Conscious State
Disorders of Consciousness
Caregivers

Treatments

Behavioral: Questionnaires
Behavioral: Coma scales
Diagnostic Test: Imaging, electrophysiology, body signals, and brain stimulation

Study type

Observational

Funder types

Other

Identifiers

NCT04798456
01KU2003 (Other Grant/Funding Number)
ERAPERMED2019-101 - PerBrain

Details and patient eligibility

About

Improved treatment of severe brain injuries has resulted in increased survival rates. While some of these patients regain consciousness after a transient state of coma, others may develop a disorder of consciousness (DoC). Diagnosis of DoC currently relies on standardized behavioral assessment. The importance of accuracy in such diagnosis cannot be overstated, as it guides critical decisions on treatment (including pain management), and could underlie end-of-life decisions. Despite this importance, current behavioral diagnosis often fails, if because of the major sensory and motor deficits associated with DoC, or because of the heterogeneous etiology and pathophysiology associated with the condition. Finally, the need for accurate diagnosis and prognosis transcends the needs of the patients alone: caregiving of these patients is very stressful, principally for the large uncertainty associated with them. Thus, more accurate diagnosis and prognosis provide major relief for caregivers, and paradoxically, even if the news is not "good". For all these reasons it is critical to developing personalized diagnosis and prognosis prediction tools that permit a stratified analysis at the single-patient level. The PerBrain Project will benefit from the multidisciplinary partners' expertise, and the unique opportunity to perform longitudinal assessments in four clinical sites through both established and novel electrophysiological, neuroimaging, and physiological techniques. Based on the collected data, the investigators will develop a multimodal personalized diagnostic tool for DoC patients using state-of-the-art computational tools, such as machine learning, in order to better determine the current state (diagnosis) and future outcome (prognosis). The overall aim of this project will provide for a better understanding of the pathophysiological mechanisms in DoC, which will, in turn, allow personalized rehabilitation strategies, and improved single-patient predictions of state and prognosis.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  • Recruitment is taking place in:

    • France, Paris, Pitie-Salpetriere Hospital;
    • Italy, Milan, Dipartimento di Cura e Riabilitazione delle Gravi Cerebrolesioni Acquisite (GCA);
    • Israel, Raanana, Loewenstein Hospital;
    • Germany, Munich: intensive care units of the University Clinic LMU Munich and Therapiezentrum Burgau
  • Inclusion criteria:

    • Disorder of consciousness (UWS and MCS) patients and their caregiver/legal guardian
    • Patient age: 18-85 years
    • Informed consent signed by legal guardian
  • Exclusion criteria:

    • Pregnancy
    • Pre-existing coma/VS/MCS
    • Continuous medical sedation (induced coma)
    • Use of barbiturates for sedation
    • Terminal malignant disease, as it increases the likelihood of not being alive for the 12-month follow-up
    • Prediction of a highly unlikely survival until the time of the 12-month follow-up due to conditions such as multi-organ failure based on the judgement of a critical care physician
    • Withdrawal of life-support
    • Palliative care setting
    • Epileptic seizures (TMS contraindication)
    • MRI contraindications (magnetic material in or on person such as pacemakers, cochlear implants, shell splinters, metal plates, certain prosthetic joints/limbs, copper-based intrauterine device, magnetic clips or stents, some large tattoos)

Trial design

150 participants in 2 patient groups

Patients with DoC
Treatment:
Diagnostic Test: Imaging, electrophysiology, body signals, and brain stimulation
Behavioral: Coma scales
Caregivers/ legal guardian of patients with DoC
Treatment:
Behavioral: Questionnaires

Trial contacts and locations

4

Loading...

Central trial contact

Benjamin Rohaut, MD/PhD; Jacobo Sitt, MD/PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems