A pilot study on the use of transcutaneous auricular vagus nerve stimulation to relieve dysmenorrhea in patients with adenomyosis and endometriosis

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AI-generated summary by claude@2026-06, 2026-06-08

This pilot study explored transcutaneous auricular vagus nerve stimulation (taVNS) in six patients with adenomyosis and endometriosis, finding it well-tolerated and effective in relieving menstrual pain at three and six months.

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AI-generated deep summary by claude@2026-06, 2026-06-12 · read from full text

This pilot study evaluated transcutaneous auricular vagus nerve stimulation (taVNS) for feasibility, tolerability, and changes in dysmenorrhea severity in six treatment-naïve reproductive-age patients (four with adenomyosis and two with unilateral ovarian endometrioma). Participants received taVNS once daily for 30 minutes over 6 months, with outcomes assessed at baseline, 3 months, and 6 months using visual analog scale (VAS) scores for dysmenorrhea, menstrual blood loss, hemoglobin, and heart rate variability (HRV) measures of vagal tone. Median dysmenorrhea VAS scores decreased significantly at both 3 and 6 months, and HRV showed a progressive improvement in vagal tone (increased RMSSD, pNN50, and high-frequency power; decreased low-frequency power and LF/HF ratio), while uterine volume, lesion size, menstrual blood loss, hemoglobin, and several blood markers did not change. The authors explicitly frame this as a small, non-randomized pilot and emphasize the need for larger randomized sham-controlled trials; this paper is centrally about endometriosis and adenomyosis — it tests taVNS as a neuromodulatory approach to relieve dysmenorrhea in patients with these conditions.

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Abstract

Adenomyosis and endometriosis are two sister diseases that cause menstrual pain and other symptoms. We have previously reported that patients with these conditions have a less active 'calm-and-rest' system and a more active 'stress-and-alert' system. Other studies have shown that a gentle, non-invasive treatment called transcutaneous auricular vagus nerve stimulation (taVNS) can safely and effectively boost the 'calm-and-rest' system in many disorders. So we wanted to see if taVNS could also help with menstrual pain caused by endometriosis and adenomyosis. We tried it in a small pilot study with four patients with adenomyosis and two patients with endometriosis. They received taVNS for six months. We found that taVNS was well tolerated and relieved their pain three and six months after taVNS. These early results are encouraging, but because the study was small, we need larger, more rigorous studies to fully know how well taVNS works for this kind of pain.
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Funding

This research was supported by grant 202440057 (JN) from the Clinical Research Project of Shanghai Municipal Health Commission.

Coi Statement

S-WG has served as a consultant or speaker within the past 12 months to E3A HealthCare, FimmCyte AG, Maipl, ReproNova, and Ziwig. Neither S-WG nor his family members hold issued stock directly or indirectly in any of these companies. S-WG holds non-exercised options in Heranova. S-WG is an Associate Editor of Reproduction & Fertility and was not involved in the review or editorial process for this paper, on which he is listed as an author. All others have nothing to declare.

Author Contributions

S-WG and XL contributed to conceptualization. S-WG and JN contributed to methodology and resources. JN and YY contributed to validation, investigation, and data curation. S-WG contributed to formal analysis, visualization, and writing of the original draft. S-WG, JN, YY, XL, and PRK reviewed and edited the manuscript. JN and XL contributed to supervision and project administration. JN contributed to funding acquisition. All authors have read and agreed to the published version of the manuscript.

Human Rights Statements And Informed Consent

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Declaration of Helsinki 1964 and its later amendments. Informed consent was obtained from all patients for being included in the study. This study was approved by the Institutional Ethics Review Board of Shanghai OB/GYN Hospital, Fudan University (No. 2024-93). Each patient enrolled in this study signed an informed consent for all the procedures and to allow data collection and analysis for research purposes.

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Outcome instruments

VAS-pain MUSA

Condition tags

endometriosisadenomyosisdysmenorrhea

MeSH descriptors

Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis Adenomyosis

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last seen: 2026-07-27T06:15:28.040536+00:00
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