NCT05992259Completed
Auricular Vagus Stimulation and STEMI
Auricular Vagus Stimulation and ST-Segment Elevation Myocardial Infarction
Source: ClinicalTrials.gov · Last updated 20 Jul 2026
Brief summary (registry, in English)
At the moment, the invasive strategy for the infarct-associated coronary artery in patients with ST-segment elevation myocardial infarction (STEMI) necessary to save the myocardium and reduce the size of the necrosis zone remains the leading one. However, despite the high efficiency of providing medical care to patients with acute coronary syndrome (ACS), there remains a high mortality and disability of this group of patients. In this regard, the search for new drug and non-drug strategies for the treatment of patients with ACS is actively continuing. Over the past decade, it has been shown that transcutaneous vagus nerve stimulation (TENS) has a cardioprotective effect both in chronic heart failure and in coronary heart disease, improves cardiac function, prevents reperfusion injury, weakens myocardial remodeling, increases the effectiveness of defibrillation and reduces the size of a heart attack. One of the methods of noninvasive stimulation of the afferent fibers of the vagus nerve is percutaneous electrical stimulation of the auricular branch of the vagus nerve. However, further studies are needed to determine whether stimulation of the tragus can improve the long-term clinical outcome in this cohort of patients.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 110 (actual)
- First submitted
- 27 Jun 2023
- Start date
- 1 Sept 2022
- Primary completion date
- 30 Mar 2026
- Lead sponsor
- Bakulev Scientific Center of Cardiovascular Surgery
- NCT number
- NCT05992259
What you commit to
- Study type: Interventional
- Participants enrolled: 110
- From 1 Sept 2022 to the primary completion date, 30 Mar 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
- Thrombolytic therapy at the prehospital stage;
Other illness
- acute heart failure III-IV;
- a history of myocardial infarction;
Other
- bradyarrhythmias;
- atrial fibrillation/flutter at the time of switching on;
- PCI/coronary artery bypass grafting (CABG) in the anamnesis.
Who the study is looking for
- patients with STEMI who have signed an informed voluntary consent to participate in the study;
- primary myocardial infarction;
- treatment in the first 12 hours from the onset of pain syndrome;
- primary PCI.
Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Scientific Research Institute Ochapovsky Regional Clinical Hospital Coordinator of this site? Confirm its status | Krasnodar | Russia | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.