About this trial
The goal of this observation study is to learn about the prediction value of combined electroencephalographic and electromyographic response in disorders of consciousness.
The main ways of stimulation is thermal and itch. Six months after inclusion in the study, patients were classified according to the Glasgow Outcome Scale Extended, (GOSE).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥18 years.
Brain damage lasts 28 to 90 days.
It meets the diagnostic criteria of unresponsive arousal syndrome/vegetative state (UWS/VS) or microconscious state (MCS).
All subjects' legal guardians sign informed consent forms.
Disqualifiers
Spinal cord T1 and above plane injury, peripheral nerve injury and so on affect nerve conduction;
The impact of injury on palms and soles of feet;
History of developmental, psychiatric, or neurological disorders prior to brain injury.
Deep sedation within 72 hours, including the use of general anesthesia.
Trial population
patients wih disorders of consciousness in xijing hospital
Trial design
Cohort
Prospective
Treatments tested in this trial
thermal stimulation
Other interventioncontact heat stimulation at 54℃
itch
Other interventionitch the sole of the foot
Treatment groups
Trial outcomes
Primary outcomes
the state of consciousness
Secondary outcomes
the score of GOSE
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
KY20242235jiangwen
Lead sponsor
Xijing Hospital
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: