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Safety and effectiveness of transcranial electro-optical synchronous stimulation device guided by brain signal quantification

Safety and effectiveness of transcranial electro-optical synchronous stimulation device guided by brain signal quantification

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044275
Enrollment
Unknown
Registered
2021-03-14
Start date
2021-03-15
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Depression

Interventions

Group 1:tNIRS stimulation
Group 2:tdcs stimulation
Group 3:TNIRS-TDCS stimulation

Sponsors

Xuanwu Hospical of Capital Medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) At least two attending doctors and above confirmed that they met the DSM-V diagnostic criteria for depressive disorder and depressive episode; 2) Aged 18 to 65 years; 3) Hamilton 17 item Depression Scale score >= 17; 4) One month before admission, the patients did not receive neuromodulation therapy such as electroconvulsive therapy and transcranial magnetic stimulation; 5) The patients did not receive any medication or took antidepressants steadily, but the therapeutic effect was not good; 6) Informed consent was signed by the patient or his family.

Exclusion criteria

Exclusion criteria: 1) There were substance abusers / addicts within 6 months before enrollment; 2) They had other mental diseases within 6 months before enrollment; 3) Patients with severe or unstable organic diseases; 4) Pregnant or lactating women; 5) HDRS-17 item 3 (suicide) score >=3; 6) The researcher thinks that there are some situations that are not suitable for participating in this study.

Design outcomes

Primary

MeasureTime frame
HDRS-17;

Countries

China

Contacts

Public ContactJianghong Liu

Xuanwu Hospical of Capital Medical University in Beijing

13341070223@163.com+86 13341070223

Outcome results

None listed

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