Arrhythmias & electrophysiology

Transcutaneous Electrical Vagus Nerve Stimulation to Suppress Premature Ventricular Contractions: A Crossover, Randomized Clinical Trial (NoVa-PVC)

JACC Clin ElectrophysiolPublished prospective, sham-controlled, single-blinded, crossover randomized clinical trial

Primary result · Median PVC burdenResult — go to the resultReduction in median PVC burden 13.4%

Authors' conclusion

LLTS effectively reduced PVC burden in patients with symptomatic PVCs refractory to medical therapy, highlighting its potential as an adjuvant therapeutic option. Larger, multicenter trials are warranted to confirm these findings and evaluate long-term outcomes [Non-invasive Vagal Stimulation for Frequent Premature Ventricular Complexes (NoVa-PVC); NCT05341544].

Study context

Population
Patients with symptomatic premature ventricular complexes (PVCs) with at least 5% daily PVC burden and who were refractory to medical therapycompleted the study and were included in the analysis, of 36 randomized patients
Participants
35 patients
Comparison
active LLTS vs sham stimulation, crossover with 8-day washout
Methodological details2-center
  • 2-center

Primary result

Median PVC burden

Reduction in median PVC burden

13.4%

P = 0.021

As reported in the abstract

Median PVC burden, as printed
10.5% [IQR: 14.4%] vs 8.59% [IQR: 8.45%]

Further findings

Heart rate variability

No significant differences in heart rate variability between the 2 groups

Baseline PVC burden

Median baseline PVC burden
12.00% (IQR: 11.4%)

Exploratory analyses

More pronounced reduction in slow heart rate-dependent PVCs and a sustained decrease in PVC burden throughout the LLTS period
  • Exploratory

Original publication

Transcutaneous Electrical Vagus Nerve Stimulation to Suppress Premature Ventricular Contractions: A Crossover, Randomized Clinical Trial (NoVa-PVC). JACC Clin Electrophysiol. Published 24 April 2025. doi:10.1016/j.jacep.2025.04.011

Summarised from the published abstract; every number is checked against it

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.