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NOT YET RECRUITING
NCT07689981
NA

The Efficacy of Transcutaneous Auricular Vagus Nerve Stimulation in Individuals With Tiletamine Use Disorder

Sponsor: Shanghai Mental Health Center

View on ClinicalTrials.gov

Summary

Participants diagnosed with tiletamine use disorder will be assigned to active or sham taVNS for 5 days. Clinical outcomes ( e.g., behavioral paradigms measures and clinical scales ) and physiological markers (e.g., EEG and ECG) will be evaluated at baseline, post-treatment, and 3-month follow-ups to determine therapeutic efficacy and mechanisms of action.

Official title: Effect of Transcutaneous Auricular Vagus Nerve Stimulation on Patients With Tiletamine Use Disorder: A Randomized Double-Blind Sham-Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-07-01

Completion Date

2028-01-01

Last Updated

2026-07-08

Healthy Volunteers

No

Interventions

DEVICE

Transcutaneous Auricular Vagus Nerve Stimulation

The stimulation duration is 40 minutes per session, administered four times daily for 5 consecutive days (20 sessions in total).

DEVICE

Sham Stimulation

Identical device appearance and parameters, with minimal sensory stimulation and no vagal activation. The treatment schedule is identical to that of the active group.

Locations (1)

Shanghai Mental Health Center

Shanghai, Shanghai Municipality, China