TREAT-PVCLow-Level Tragus Stimulation for Frequent Premature Ventricular Contractions
Low-level tragus stimulation
+ Sham stimulation
Cardiac Conduction System Disease+5
+ Arrhythmias, Cardiac
+ Cardiovascular Diseases
Treatment Study
Summary
Study start date: March 15, 2021
Actual date on which the first participant was enrolled.This study focuses on a common type of irregular heartbeat known as Premature Ventricular Contraction (PVC). PVCs can potentially harm patients by increasing the risk of heart disease, triggering other serious heart rhythms, and worsening existing heart conditions. Currently, treatment for PVCs primarily involves medication, but effectiveness varies greatly among individuals. The study aims to explore a new, non-invasive method called low-level tragus stimulation (LLTS) to manage PVCs. This method involves stimulating the vagus nerve through the tragus of the ear, which has shown promise in reducing symptoms related to heart conditions and other disorders. The study is designed as a randomized, single-blind trial involving 100 patients. Participants are divided into two groups: one receiving active LLTS and the other receiving a sham treatment. The active LLTS is administered using a device called the Parasym device, which stimulates the vagus nerve through an ear clip attached to the tragus. The sham treatment involves attaching the clips to the earlobe, which does not affect the vagus nerve. Patients' heart activity is monitored at baseline, 3 months, and 6 months using a non-invasive, adhesive ECG patch. The study measures the burden of PVCs, or the percentage of premature ventricular beats in total heartbeats. Additionally, it evaluates heart rate variability, quality of life, skin sympathetic nerve activity, and serum cytokine levels at baseline and follow-up.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.100 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ShamStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
The First Affiliated Hospital of Nanjing Medical University
Nanjing, ChinaOpen The First Affiliated Hospital of Nanjing Medical University in Google Maps