NCT06784583Completed
A Study on Transcutaneous Vagus Nerve Stimulation in Perioperative Period of Percutaneous Coronary Intervention
A Study on Transcutaneous Vagus Nerve Stimulation in Perioperative Period of Percutaneous Coronary Intervention: A Randomized Clinical Trial
Source: ClinicalTrials.gov · Last updated 3 Dec 2025
Brief summary (registry, in English)
The goal of this clinical trial is to study the effect of transcutaneous auricular vagus nerve stimulation on perioperative blood pressure. The main question it aims to answer is: •Wether the transcutaneous auricular vagus nerve stimulation have advantages in perioperative blood pressure elevation. Participants will sign an informed consent form, collaborate with data collection, and are randomly divided into two groups(1:1) to accept the intervention measures from corresponding groups. Researchers will record the perioperative blood pressure and compare intervention group with sham group to see if there is any difference in perioperative blood pressure.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 480 (actual)
- First submitted
- 10 Jan 2025
- Start date
- Sept 2023
- Primary completion date
- Jan 2025
- Lead sponsor
- Guozhe Sun
- NCT number
- NCT06784583
What you commit to
- Study type: Interventional
- Participants enrolled: 480
- From Sept 2023 to the primary completion date, Jan 2025
- 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
- Patients participating in clinical trials of other drugs or medical devices
Other illness
- Patients with acute myocardial infarction
- Patients with heart failure of NYHA class III - IV
- Patients with a medical history of hyperthyroidism
- Patients with infections and fever
- Patients who are unable to cooperate due to mental and psychological disorders (such as mania, depression)
Lab values
- With an estimated glomerular filtration rate (eGFR) of less than 60 ml/min/1.73m² on admission
Other
- Patients with atrial fibrillation (indicated by definite medical history or electrocardiogram on admission)
- Patients with subclavian artery occlusion (indicated by definite medical history or a difference in systolic blood pressure of more than 20 mmHg between the two upper limbs)
- Patients with tinnitus and vertigo
- Pregnant women or patients who are attempting to get pregnant
- Patients deemed unsuitable by the researchers to participate in this clinical trial
Who the study is looking for
- Ages between 18 and 70 years old, regardless of gender
- Patients with indications for coronary artery stent implantation
- hypertension history
- Voluntarily participate and sign an informed consent form
Age in the registry: 18 years to 70 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 |
|---|---|---|---|
| First Hospital of China Medical University Coordinator of this site? Confirm its status | Shenyang | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.