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Clinical Trial

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

NCT: NCT07689981 · NOT_YET_RECRUITING

NCT IDNCT07689981
StatusNOT_YET_RECRUITING
Start Date2026-07-01
Completion2028-01-01
SponsorShanghai Mental Health Center (OTHER)
First posted
Last updated

Brief 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 Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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