Clinical Trial

Mechanisms of Transcutaneous Auricular Vagus Nerve Stimulation in Depression

Study acronym: AddVNS
Recruiting
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Summary
Invasive vagus nerve stimulation (VNS) is an approved treatment of treatment-resistant depression (TRD) in Europe and in USA. Because of the associated possible surgical complications as well as side effects, invasive VNS is applied limitedly in the treatment of depression. Transcutaneous auricular VNS (tVNS), on the other hand, is a non-invasive alternative to traditional invasive VNS. tVNS is still considered an experimental treatment for depression. This is due to the limited high-quality evidence from randomized clinical studies, the not yet fully understood biological mechanisms of action, along with overall limited knowledge about the optimal stimulation parameters. To address these issues, the AddVNS study was initiated. The AddVNS study intends to recruit n=86 patients of the Max Planck Institute of Psychiatry with depression. The patients participating in the AddVNS study are going to receive either tVNS or sham tVNS for a period of 6 weeks. The primary objective of the study is to identify biological, psychological, socio-economic, and clinical biomarkers associated with treatment progression and response to treatment in patients with depression undergoing tVNS. To achieve this, an exploratory design with an assessment of many different parameters including psychophysiology, imaging, blood-based multi-omics, microbiome, psychometrics and neuropsychology will be used.
Trial Details
NCT Number NCT07022171
Lead Sponsor Max-Planck-Institute of Psychiatry
Conditions Depressive Disorder, Bipolar Disorder
Enrollment 86 participants
Start Date 2025-03-18
Primary Completion 2030-03-17 (estimated)
Study Completion 2030-03-17 (estimated)
Updated on ClinicalTrials.gov 2025-06-15