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Exploring the efficacy of high-precision transcranial direct current stimulation in patients with minimal consciousness in combination with cardiopulmonary coupling technique

Exploring the efficacy of high-precision transcranial direct current stimulation in patients with minimal consciousness in combination with cardiopulmonary coupling technique

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073085
Enrollment
Unknown
Registered
2023-06-30
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

disorders of consciousness

Interventions

Trial 1:transcranial direct current stimulation of 2 mA for 20 minutes in the left DLPFC area
Trial 2:transcranial direct current stimulation of 2 mA for 20 minutes in the right DLPFC area
Control:left/right DLPFC area sham stimulation

Sponsors

Huashan hospital, rehabilitation department, No12 Wulumuqi middle Rd, Jingan district, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients whose immediate family members volunteered to participate, signed the informed consent form on their behalf, and were able to complete the trial according to the protocol; (2) Diagnosis of MCS according to the CRS-R score; (3) Right-handedness; (4) having stable vital signs; (5) Age 18-80 years; (6) No use of neuromuscular blocking agents and sedatives within 24 hours prior to study participation; (7) No observed improvement in the state of consciousness within 1 week prior to the start of the study; (8) Duration of impaired consciousness was at least 28 days.

Exclusion criteria

Exclusion criteria: (1) Known pre-existing severe neurocognitive degenerative disease; (2) Metal implants in the head; (3) Craniectomy beneath the stimulated area (i.e., prefrontal cortex); (4) Previous history of epilepsy or current uncontrolled epilepsy; (5) Previous treatment with transcranial electrical stimulation.

Design outcomes

Primary

MeasureTime frame
the Coma Recovery Scale–Revised;

Secondary

MeasureTime frame
Glasgow Outcome Scale;CPC cardiopulmonary coupled sleep monitoring;Electroencephalogram;

Countries

China

Contacts

Public ContactWu Yi

Shanghai Huashan Hospital

Wuyi4000@163.com+86 189 3082 8028

Outcome results

None listed

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