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Effects of transcranial direct current stimulation in perioperative depression in patients with breast cancer surgery

Effects of transcranial direct current stimulation in perioperative depression in patients with breast cancer surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104410
Enrollment
Unknown
Registered
2025-06-17
Start date
2024-12-17
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Perioperative depression

Interventions

tDCS Group:Transcranial DC stimulation
sham tDCS Group:sham Transcranial DC stimulation

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate in the trial and sign the informed consent form; 2. Age>=18 years old patients undergoing elective breast cancer surgery; 3. ASA Class I-III; 4. Hamilton Depression Rating Scale-17-item score >=7.

Exclusion criteria

Exclusion criteria: 1.Refusal to sign the consent form; 2. History of mental illness; 3. Craniocerebral or scalp injury; 4. Severe cardiovascular or cerebrovascular diseases; 5. Metal implants in the body; 6. Use psychotropic drugs within 2 weeks before the operation; 7. Cannot cooperate with the depression scale evaluation.

Design outcomes

Primary

MeasureTime frame
Beck Depression Inventory Score;Hamilton Depression Rating Scale, HAMD-17;

Secondary

MeasureTime frame
Postoperative delirium;Rest Vision Analog Scale Rating;Pittsburgh sleep quality index;Activity Visual Analog Scale Rating;Nausea and vomiting;

Countries

China

Contacts

Public ContactZanwang

Xuzhou Central Hospital

840547858@qq.com+86 17712986638

Outcome results

None listed

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