Skip to content

EEG Characteristics in Patients with Prolonged Disorders of Consciousness Treated by Transcranial Direct Current Stimulation

EEG Characteristics in Patients with Prolonged Disorders of Consciousness Treated by Transcranial Direct Current Stimulation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093590
Enrollment
Unknown
Registered
2024-12-09
Start date
2023-10-02
Completion date
Unknown
Last updated
2024-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disorders Of Consciousness

Interventions

Minimally Conscious State:Provide conventional physical therapy such as traditional rehabilitation acupuncture, positioning, range of motion exercises, tilt table training, rehabilitation cycling, res
Unresponsive Wakefulness Syndrome:Provide conventional physical therapy such as traditional rehabilitation acupuncture, positioning, range of motion exercises, tilt table training, rehabilitation cycl
Control group:Provide conventional physical therapy such as traditional rehabilitation acupuncture, positioning, range of motion exercises, tilt table training, rehabilitation cycling, respiratory reh

Sponsors

Binzhou Medical University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. GCS score between 4 and 8; 2. 28 days post-onset or post-injury; 3. Age >= 18 years; 4. Known etiology of consciousness disorder; 5. No neurological deficits prior to brain injury; 6. Diagnosed with UWS/VS or MCS based on at least two CRS-R assessments during screening; 7. Informed consent obtained from family members.

Exclusion criteria

Exclusion criteria: 1. Pregnancy; 2. Uncontrolled epilepsy, defined as seizures within 4 weeks prior to enrollment; 3. Intracranial metal implants; 4. Pacemaker; 5. Craniotomy under the stimulation site; 6. Use of sedatives or medications considered to interfere with brain stimulation, such as sodium or calcium channel blockers or NMDA receptor antagonists; 7. Concurrent participation in any other therapeutic clinical trials.

Design outcomes

Primary

MeasureTime frame
Coma recovery scale-revised;

Secondary

MeasureTime frame
Power Spestrum;Functional Connectivity;

Countries

China

Contacts

Public ContactHongwei Li

Binzhou Medical University Hospital

drlihongwei@163.com+86 186 5439 7805

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026