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NCT05230628Active, not recruiting

Auricular Vagus Stimulation in Obesity

The Effectiveness of Transcutaneous Electrical Nerve Stimulation of the Auricular Branch of the Vagus Nerve in Loss Weight and Improving the Quality of Life in Patients With Obesity

Source: ClinicalTrials.gov · Last updated 3 Sept 2025

Brief summary (registry, in English)

Transcutaneous vagus nerve stimulation (TENS) involves stimulation of the left and/or right auricular branch of the vagus nerve with low-frequency electrical impulses. In recent years, the possibilities of using this technology in chronic conditions characterized by immune and metabolic dysregulation have been studied. The aim of this study is to investigate the effectiveness of TENS in reducing weight and improving quality of life in patients with various degrees of obesity.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
131 (actual)
First submitted
28 Jan 2022
Start date
4 Apr 2022
Primary completion date
31 Jan 2026
Lead sponsor
National Medical Research Center for Therapy and Preventive Medicine
Diseases
Obesity
NCT number
NCT05230628

What you commit to

  • Study type: Interventional
  • Participants enrolled: 131
  • From 4 Apr 2022 to the primary completion date, 31 Jan 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Presence of an electrically, magnetically or mechanically activated implant, an intracerebral vascular clip, or any other electrically sensitive support system.

Other illness

  • Cardiac arrhythmias: bradyarrhythmias, Atrioventricular blockades of any degree;

Other

  • Taking beta blockers;
  • The endocrine nature of obesity;
  • Expected technical difficulties when using the device on the part of the patient;
  • Pregnant or plan on becoming pregnant or breastfeeding during the study period;

Who the study is looking for

  • Adult patients with grade 1-2 nutritional obesity who are willing and able to give informed written consent to participate in the study, are on sinus rhythm and are not taking any antiarrhythmic drugs, including beta-blockers.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Medical Research Center for Therapy and Preventive Medicine
Coordinator of this site? Confirm its status
MoscowRussiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.