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The cohort study on the auricular electro-acupuncture treating the Treatment-resistant depression

Neuroimaging study of the emotion-cognitive circuits regulated by transcutaneous auricular vagus nerve stimulation on the Treatment-resistant depression

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014277
Enrollment
Unknown
Registered
2018-01-02
Start date
2018-01-16
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

Treatment-resistant depression

Interventions

Two groups:Auricular electro-acupuncture plus Sertraline versus Sertraline alone

Sponsors

Guang An Men Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic standard "Depressive episode, the Handbook of Mental Disorders Statistics and Diagnosis, DSM-5"; 2. The total score of Hamilton Depressive Scale (HAMD-24) =17 points; 3. With reference to Thase and Rush criteria, the TRD must meet one of the following criteria: (1) Based on the medical history,at least Two kinds of adequate, full course (>3 months) of different structures of antidepressant treatment ineffective; (2) in a sufficient amount of antidepressants,enough treatment (>3 months) treatment is invalid, for another HAMD-24 scores 6 weeks); (3) For patients with first episode, two different structures of antidepressants in sufficient quantity and duration of treatment (> 6 weeks) ineffective. 4. Meet the TRD diagnostic criteria, aged 18-55 years of patients with Treatment-resistant depression, male or female; 5. Clinical examination and related laboratory tests showed no abnormalities; 6. Right hand; 7. Not previously taken the medicines of which used in this study; 8. Agree and sign informed consent form.

Exclusion criteria

Exclusion criteria: 1. Bipolar affective disorder, schizoaffective disorder,schizophrenia or other psychotic disorders; 2. A history of seizures or strong positive family history of epilepsy; 3. Serious physical illness or organic brain disease; 4. Serious Impotence,suicide or self-injury risk; 5. History of abuse of alcohol dependence or other active substances, while taking other psychotropic drugs (such as antipsychotics,mood stabilizers or central stimulants, etc.); 6. pregnant, preparing for pregnancy or Lactation; 7. past the body of metal implants; 8. into the group before January received a modified electrical shock or transcranial magnetic, DC stimulation therapy and other physical therapy; 9. included in the study before January have participated Other drug research in clinical trials.

Design outcomes

Primary

MeasureTime frame
Hamilton Depressive Scale, HAMD-24;

Countries

China

Contacts

Public ContactJiliang Fang

Guang An Men Hospital of China Academy of Chinese Medical Sciences

fangmgh@163.com+86 13683338202

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026