SAFETY & TOLERABILITYSYSTEMATIC REVIEW & META-ANALYSIS2022

Safety and tolerability of taVNS

Safety of Transcutaneous Auricular Vagus Nerve Stimulation (taVNS): A Systematic Review and Meta-Analysis

This systematic review and meta-analysis examined safety reporting across 177 taVNS studies involving 6,322 participants.

Study in plain English

A broad view of reported taVNS safety

The review assembled safety information across a large and diverse body of taVNS research. Its findings are useful, but incomplete adverse-event reporting limits certainty.

Research scale

The review included 177 studies involving 6,322 participants.

Overall adverse-event risk

The meta-analysis found no difference in overall adverse-event risk between active taVNS and control conditions.

Reporting matters

Adverse-event reporting was incomplete across a substantial proportion of the included literature.

Study design

How the research was structured

Study type

Systematic review and meta-analysis

Included studies

177 studies

Participants

6,322 participants

Main focus

Adverse events, safety reporting, and tolerability

Key findings

What the study reported

Overall risk comparison

The meta-analysis found no difference in the overall risk of developing an adverse event between active taVNS and control conditions.

Frequently reported events

The most frequently reported adverse events included ear pain, headache, and tingling.

Serious adverse events

The authors found no causal relationship between taVNS and serious adverse events in the reviewed research.

Important context

Limitations remain part of the finding.

Adverse-event reporting was incomplete across a substantial proportion of the included studies.

Absence of an identified causal relationship is not the same as proof that every taVNS protocol is risk-free.

Safety findings from a broad literature cannot automatically be transferred to every device, stimulation site, protocol, or user.

What this study does not show

The review does not establish that taVNS has no risks.

It does not replace product-specific contraindications, warnings, instructions, or professional advice.

It is not clinical safety evidence for the Neuvago device itself.

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Research boundary

This page summarizes peer-reviewed research for educational purposes. The study provides scientific context for the taVNS field and should not be interpreted as clinical evidence for the Neuvago device, medical advice, diagnosis, or treatment guidance.