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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01620957
Other study ID # C11-55 Inserm
Secondary ID 2012-A00009-34
Status Completed
Phase
First received
Last updated
Start date July 10, 2012
Est. completion date July 2017

Study information

Verified date August 2021
Source Institut National de la Santé Et de la Recherche Médicale, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Several studies in healthy volunteers have suggested that the synchronized functional connectivity in the DMN (Deafult-Mode Network) would sustain the mental content at rest, and when required, a switch in the activity between the DMN and other networks involved in specific congnitive functions, would occur. This interaction permit to make the hypothesis, that baseline brain activity is likely to shape our ongoing " stream of consciousness " and could correlate with conscious perception. The investigators hypothesized that DMN connectivity strength would be related to the level of consciousness of brain-damaged patients. The investigators will follow severely brain-injured patient in coma. Clinical examination using standardized behavioural scales: FOUR score (Full Outline of UnResponsivess), Coma Recovery Scale-Revised); and brain imaging assessesments using MRI (functional and anatomical connectivity, cortical thickness) will be performed at: 3 to 30 (visit 1), and 60 (visit 2) days after insult. If patient recover a normal conscious state between 30 and 60 days, an additional clinical and brain imaging assessment will be performed to identify related changes in brain activity (visit 1*) Monitoring of vital parameters will be performed in patients by a senior anaesthesiologist throughout the experiment.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Brain-damaged patients in coma (trauma or anoxic origin). - Male and female, ranging in age from 18 to 75 years. Exclusion Criteria: - Withdrawal of consent from the patients (or the persons having legal responsibility for them). - Sedation or general anaesthesia during assessement period (< 24 hours). - MRI contraindications

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Institut National de la Santé et de la Recherche Medicale, U825 Toulouse Haute Garonne

Sponsors (3)

Lead Sponsor Collaborator
Institut National de la Santé Et de la Recherche Médicale, France Association des Traumatisés du Crane et de la Face, Paris, France, University Hospital, Toulouse

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of DMN resting state fMRI connectivity between 1 and 2 month after severe brain injury To date, the functional significance of DMN resting state connectivity patterns remain unclear. We hypothesized that DMN connectivity strength would be related to the level of consciousness of non-communicative brain-damaged patients, as assessed by standardized behavioural scales (FOUR score, CRS-R). Furthermore, we expected that a disruption of functional connectivity in the DMN could predict brain-damaged patient's recovery. VISIT1 = coma state (an expected average of 3 to 30 days after brain injury), VISIT2 = recovery phase (an expected average of 30 to 60 days). Finally, in case of full recovery during the recovery phase an additional assessment will be performed (VISIT1*)
Secondary Compare functional and structural DMN connectivity between 1 and 2 month after severe brain injury Functional DMN connectivity will be investigated using probabilistic independent component analysis. Structural connectivity counterpart, will be assessed by diffusor tensor imaging and cortical thickness. VISIT1 = coma state (an expected average of 3 to 30 days after brain injury), VISIT2 = recovery phase (an expected average of 30 to 60 days). Finally, in case of full recovery during the recovery phase an additional assessment will be performed (VISIT1*)
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