← Eichor
Study identifier: NCT07021508 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Efficacy and Safety Assessment of Temporal Interference Stimulation to Improve Bipolar Depression

Condition: Bipolar Depression  ·  Sponsor: First Affiliated Hospital of Zhejiang University

PhaseNA
Planned participants160
Who can joinAll sexes, 18 Years to 45 Years
Healthy volunteersNo

About this study

The aim of this study was to explore the efficacy and safety of temporal interference stimulation to improve bipolar depression, as well as to explore the corresponding neuroimaging mechanisms using magnetic resonance and electroencephalogram to provide novel intervention protocols and objective indicators of efficacy prediction for depressive episodes in bipolar disorder.

This description comes directly from the study's public registry record.

Talk to the study team

Shaohua Hu, PhD  ·  0571-87232984  ·  dorhushaohua@zju.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Psychiatry, First Affiliated Hospital of Zhejiang UniversityHangzhou, Zhejiang, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07021508