Migrainepatiënten vinden verlichting door het gebruik van transcutane nervus vagus stimulatie (tNVS).

Migraine patients find relief through the use of transcutaneous vagus nerve stimulation (tNVS).

Can Transcutaneous Vagus Nerve Stimulation (tVNS) Help Migraine?

A Look at Science

Migraines are much more than just headaches—they are complex neurological attacks that disrupt the daily lives of millions of people worldwide. Because traditional treatments don't always provide relief, researchers are increasingly turning to innovative neuromodulation techniques. One of these methods, transcutaneous vagus nerve stimulation (tVNS), is gaining attention for its potential to reduce migraine symptoms. But how effective is it, and what does the latest research say?

What is tVNS?

The vagus nerve is a vital nerve that communicates between your brain and body, influencing pain, inflammation, and even mood. tVNS is a non-invasive technique that uses mild electrical stimulation of the vagus nerve through the skin, usually near the ear or neck. Unlike surgically implanted devices, tVNS is external, making it attractive to many patients.

The Science: What Do the Studies Say?

Early Research and Mechanisms of Action

Early studies (Yamakami et al., 2000; Møller, 2003) investigated how modulating cranial nerves can influence neurological symptoms, including pain and tinnitus. This foundational work formed the basis for using the vagus nerve in migraine treatment.

Effectiveness in Migraine

Several clinical studies and reviews investigated tVNS in migraine:

Barbanti et al. (2017) (PubMed) showed that tVNS can significantly reduce the frequency and intensity of migraine, especially in patients who did not respond to conventional medication.

Straube et al. (2015) (PMC) reported that regular tVNS sessions reduced the number of migraine days per month and improved quality of life.

Silberstein et al. (2016) (PMC) conducted a randomized controlled trial showing that tVNS is safe, well-tolerated, and effective as add-on therapy for acute migraine attacks.

How Does tVNS Work for Migraine?

tVNS appears to influence brain areas involved in pain processing and inflammation (Frangos et al., 2015). By activating the vagus nerve, tVNS can suppress the release of pro-inflammatory neuropeptides and dampen abnormal pain signals in the brainstem and cortex (Yakunina et al., 2017; Kraus et al., 2007).

Safety and Side Effects

The safety profile of tVNS is favorable. Most reported side effects are mild, such as skin irritation or tingling at the stimulation site (Kreuzer et al., 2012). Serious side effects are rare, making tVNS a promising option for people with difficult-to-treat migraines.

Beyond Migraine: Overlap with Tinnitus

Interestingly, many of the same neural circuits involved in migraines are also involved in tinnitus—a persistent ringing or buzzing in the ears. Studies show that tVNS can also help tinnitus patients (Lehtimäki et al., 2013; De Ridder et al., 2014), suggesting a broader role for neuromodulation in neurological disorders.

The Future of tVNS in Migraine Care

While tVNS is not a miracle cure, the growing body of scientific evidence supports its use as a safe, non-invasive, and effective option for many migraine sufferers—especially those who don't respond to standard treatments. Ongoing research refines stimulation protocols and explores personalized approaches, with the hope that migraines will become less burdensome in the future.

Transcutaneous vagus nerve stimulation is developing into a valuable tool in the fight against migraine. If you or someone you know struggles with chronic migraines, it might be worth discussing tVNS with a healthcare professional. As research progresses, we can expect even more refined and effective neuromodulation treatments in the near future.

References

1. Yamakami et al., 2000

2. Møller, 2003

3. Barbanti et al., 2017

4. Yakunina et al., 2017

5. Frangos et al., 2015

6. Kraus et al., 2007

7. Kreuzer et al., 2012

8. Silberstein et al., 2016

9. Straube et al., 2015

10. Lehtimäki et al., 2013

11. De Ridder et al., 2014

Back to blog