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The efficacy and safety of nonconvulsive electrotherapy in treatment-resistant depression

Mechanism of Glu/GABA Balance in reducing Ketafol Anesthesia ECT-Induced learning and memory impairment with nonconvulsive electrotherapy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085714
Enrollment
Unknown
Registered
2024-06-17
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Treatment-resistant depression

Interventions

Nonconvulsive electrotherapy group:Nonconvulsive electrotherapy
Healthy control group:None

Sponsors

the Affiliated Brain Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for TRD Patients: ?Meets the DSM-V diagnostic criteria for depression through the Structured Clinical Interview for DSM Disorders (SCID); ?Meets the TRD criteria: ineffective treatment with at least two different classes of antidepressants at adequate dosage and duration; ? Age between 18 and 45 years, right-handed; ?At least a junior high school education, IQ > 70; ?HAMD-17 total score = 24 points; ?Both the patient and the guardian have completed the informed consent process. Inclusion Criteria for the Healthy Control Group: ?Matched with the subjects mentioned above in terms of age, gender, and educational level. ?No family history of psychiatric disorders. ?Does not meet the diagnostic criteria for any psychiatric disorders based on SCID-IV screening. ?The subject has signed an informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion Criteria for TRD Patients: ?Meets the DSM-IV Axis I diagnostic criteria for other psychiatric disorders; ?Currently has severe physical or neurological diseases; ?Has a history of stimulant, narcotic, or sedative-hypnotic drug dependence; ?Concurrently taking other medications that affect the evaluation of treatment efficacy, such as neuroleptics; ?Women who are pregnant or breastfeeding; ?Those with contraindications for MEG or MRI scans; ?Considered unsuitable for ketafol anesthesia ECT treatment by the attending physician, such as those allergic to esketamine. Exclusion Criteria for the Healthy Control Group: ?Contraindications for MEG or MRI scanning. ?Current severe physical or neurological diseases. ?Women who are pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frame
Response rate;

Secondary

MeasureTime frame
Remission rate;Neurocognitive function;

Countries

China

Contacts

Public ContactZheng Wei

the Affiliated Brain Hospital of Guangzhou Medical University,

zhengwei0702@163.com+86 159 2082 9484

Outcome results

None listed

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