NCT02798588

Brief Summary

In last decades, several advances in the neuro-intensive management have lead to decrease mortality in Intensive Care Units. A significant morbidity remains as patients survive after a traumatic coma with uncertain quality of awakening and a high risk of functional disability. Predicting awareness recovery and functional disability of those who will awake constitutes a major challenge to inform patients' relatives, to give the best chances in terms of rehabilitation resources or to adapt intensive cares to a reasonable level. Tools currently available are not sufficient neither to predict bad awakening outcome nor to predict good functional outcome. In many countries, life's support cessation is a constant call for robust evaluation as soon as possible in ICU but it is mandatory to reach a positive predictive value of non-awaking close to 100%. Many clinical, electro-physiological, biological, radiological and functional parameters have been conducted with comatose patients assuming the purpose to predict outcome. Regarding unfavourable outcome, the gold standard is the abolition of the N20 component of somatosensory evoked potentials but the specificity is high enough only for patients with anoxic coma. Several neurophysiological markers such as MMN, P300 are correlated to a favourable outcome but the sensitivity and specificity remains low for patients who suffered a severe traumatic brain injury. New Diffusion Tensor imaging sequences provide complementary information to detect small structural lesions (diffuse axonal lesions). Recently, functional MRI analyzing Resting State has also been proposed as a prognostic marker during coma. PET using Fluoro-Desoxy-Glucose is able to assess the metabolism in key regions of the awakening network in either anaesthesia or sleep. Recent studies have reported interesting results at the chronic stage but to knowledge, these tools have only been used to address pathophysiology's issues and never to improve coma prognosis at the initial stage. The investigators hypothesize that the heterogeneity of the population requires a global and accurate assessment of the central nervous system, combining structural, metabolic and functional information in order to refine the prognosis. The protocol integrates in one-sequence most radiological markers of brain injury within a unique PET-MRI in Lyon. The most relevant originality of the study consists in confronting FDG-PET and MRI sequences to a large clinical, electrophysiological and biological battery. The added clinical value would be to question the synergistic effect of each parameter and to find out which ones are the most useful for awakening prediction, as they have not been compared in a multi-parametric database. PET-MRI, as a new device combining physiological and prognostic questioning, allows us:

  • to implement a more integrative physio-pathological analysis
  • to avoid the cofounding effect of awareness' fluctuations in recording simultaneously multiple functional imaging techniques. The RS will be analyzed at 2 epochs in order to assess the stability of brain connectivity, related to neuronal activity (glucose metabolism) and brain perfusion.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2017

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 27, 2016

Completed
18 days until next milestone

First Posted

Study publicly available on registry

June 14, 2016

Completed
8 months until next milestone

Study Start

First participant enrolled

February 16, 2017

Completed
3.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 4, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 4, 2020

Completed
Last Updated

March 7, 2022

Status Verified

March 1, 2022

Enrollment Period

3.3 years

First QC Date

May 27, 2016

Last Update Submit

March 4, 2022

Conditions

Keywords

comaprognosiscomparative studyfunctional imagingPET-MRIelectrophysiology

Outcome Measures

Primary Outcomes (4)

  • Analysis of feasibility (pilot study) with Number of patients included during a 12-months period

    at 12 months

  • Analysis of feasibility (pilot study) with ratio of patient included vs patient admissible according to the screening

    at 12 months

  • Analysis of feasibility (pilot study) with respect of deadline for completion of PET MRI

    at 12 months

  • Analysis of security (pilot study) with tolerance of the PET-MRI

    at 12 months

Secondary Outcomes (3)

  • Unfavorable clinical evolution towards awareness (dichotomic criteria : absence of awareness with functional communication)

    at 12 month

  • Unfavorable clinical evolution in absence of awareness (ordinal criteria within unfavorable outcome) with Coma Recovery Scale-Revised

    at 12 month

  • Functional clinical evolution in presence of awareness (ordinal criteria within favorable outcome) according to Glasgow Outcome Scale (GOS)

    at 12 month

Study Arms (1)

Comatose patients in ICU

EXPERIMENTAL
Radiation: PET-MRI

Interventions

PET-MRIRADIATION

18Fluoro-Desoxy-Glucose's infusion for PET (glucose neural metabolism assessment, with quantitative information permitted by radioactivity monitoring through arterial catheter ; dosage = 1,5 MBq/Kg + 18,5 MBq as loading dose 5 min= Outside the scanner, Installation and movement management: Curare+/- sedative injection with standardized routine care protocol 10 min= Outside the scanner, Starting PET continuous acquisitionT= 0, Morphological MRI sequences- 3DT1, 3DFlair, T2SE, T2 HR on brainstem, Susceptibility and simple Diffusion Weighted Imaging-Specifically dedicated MR sequences based upon clinical issues 25 min, MRI in Resting state N°1 (global short-term functional connectivity)13 min, MRI DTI acquisition, 64 directions, sensitive to white matter injury 8 min, IRM in 2D-Arterial Spin Labelling:Quantitative Cerebral blood flow information (no Gadolinium)-\>8 min, IRM in Resting state 2 (repeated occurrence to assess stationarity) 13 min, End of PET continuous acquisition

Comatose patients in ICU

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients presenting either vascular or traumatic lesions
  • Patients with no response to simple command 48h after sedation's cessation
  • Patients included between 7 days (to reduce the effect of early oedema) and 30 days after the coma (to control the homogeneity of our cohort)
  • Patients included between 18 and 75 years old, to limit the risk of care withdrawal for poor previous medical condition
  • Patients evaluated by a global electrophysiological assessment at beside in ICU in a short delay before or after PET-MRI

You may not qualify if:

  • Patient with an associated anoxic encephalopathy
  • Patients with contra-indication to MRI
  • Patients with hypersensibility to the active molecules (FDG) or to one of this excipient
  • Pregnant women
  • Minor patients
  • Patients under legal protection
  • Patients not affiliated to French health care system
  • Patients in poor medical condition (hemodynamic, respiratory instability)
  • Patients moribund or with previous decision of care withdrawal
  • Absence of relatives to give written consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Réanimation polyvalente neurologique Hôpital Neurologique HCL

Bron, 69500, France

Location

MeSH Terms

Conditions

Coma

Condition Hierarchy (Ancestors)

UnconsciousnessConsciousness DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Florent GOBERT, MD

    Réanimation polyvalente neurologique Hospices Civils de Lyon

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 27, 2016

First Posted

June 14, 2016

Study Start

February 16, 2017

Primary Completion

June 4, 2020

Study Completion

June 4, 2020

Last Updated

March 7, 2022

Record last verified: 2022-03

Data Sharing

IPD Sharing
Will not share

Locations