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Canceled by the investigator. Effectiveness of rTMS in stimulating the V1 area of visual cortex versus classical target area in patients with depression: a randomized, double-blind, non-inferiority trial

Effectiveness of rTMS in stimulating the V1 area of visual cortex versus classical target area in patients with depression: a randomized, double-blind, non-inferiority trial

Status
Unknown
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026204
Enrollment
Unknown
Registered
2019-09-26
Start date
2019-10-01
Completion date
Unknown
Last updated
2023-02-13

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

Conditions

depression

Interventions

1:rTMS therapy (L-DLPFC)+ Escitalopram oxalate tablets (10mg/d)
2 :rTMS therapy (left V1 area) + Escitalopram oxalate tablets (10mg/d)

Sponsors

Zhongda Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Meet diagnostic criteria for depression; 2. Show a 24-item Hamilton Rating Scale for Depression (HRSD-24) score of at least 18; 3. Aged 18-55 years; 4. Willing to sign informed consent and be able to comply with the research plan; 5. Without obvious intelligent disorder and could understand the follow-up questionnaire survey.

Exclusion criteria

Exclusion criteria: 1. Individuals meet or met the following conditions: schizophrenia, delusional disorder, bipolar affective disorder, dementia, amnesiac, or other serious cognitive impairments, impaired mental developments, mental disorders caused by physical illness or substance abuse; 2. With the history of brain trauma or other known pathological changes of the central nervous system; 3. Psychotic symptoms or suicidal behavior during depressive episodes; 4. With endocrine and blood disease or significant abnormalities in heart, liver and kidney functions; 5. Have received the systematic treatment with elector-shock or rTMS; 6. Being treated with an antidepressant other than escitalopram and unwilling to receive a dressing change; 7. There are contraindications to rTMS or brain magnetic resonance.

Design outcomes

Primary

MeasureTime frame
HRSD-24 score;adverse events scale;

Secondary

MeasureTime frame
Montgomery Depression Rating Scale;Beck Suicide Ideation Scale;Life Event Scale;mini-mental state examination;Montreal Cognitive Assessment;Emotional-Stroop task;electroencephalogram;visual evoked potential;Event-related potential P300;

Countries

China

Contacts

Public ContactZhijun Zhang

Zhongda Hospital

janemengzhang@vip.163.com+86 13851687583

Outcome results

None listed

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