Physiological and Molecular Mechanisms of Transcutaneous Auricular Vagus Nerve Stimulation in Depression

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• age 18-65 years, legally competent and able to provide informed consent;

• diagnosis of a depressive episode (MDD or bipolar disorder) according to DSM 4/DSM 5 or ICD-10/ICD-11;

• signed informed consent documents for the AddVNS study;

• signed informed consent and participation in the biobanking project of MPIP;

• use of a safe contraceptive method

Locations
Other Locations
Germany
Max Planck Institute of Psychiatry
RECRUITING
Munich
Contact Information
Primary
Evangelos Kokolakis, MD
ambulanz@psych.mpg.de
0049-89-30622-1000
Backup
Iven-Alex von Mücke-Heim, MD, MSc
ambulanz@psych.mpg.de
0049-89-30622-1000
Time Frame
Start Date: 2025-03-18
Estimated Completion Date: 2030-03-17
Participants
Target number of participants: 86
Treatments
Experimental: tVNS-arm (transcutaneous auricular vagus nerve stimulation)
Half of the patients are randomized to the arm receiving transcutaneous auricular vagus nerve stimulation in addition to their regular treatment for a period of six weeks
Sham_comparator: sham tVNS-arm (sham transcutaneous auricular vagus nerve stimulation)
Half of the patients are randomized to the arm receiving sham transcutaneous auricular vagus nerve stimulation in addition to their regular treatment for a period of six weeks. The procedures for sham tVNS will be identical to tVNS, with the only exception that the sham tVNS will be performed with no current output
Related Therapeutic Areas
Sponsors
Leads: Max-Planck-Institute of Psychiatry

This content was sourced from clinicaltrials.gov