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Clinical Application of Vagus Nerve Stimulation Combined With Immunoregulatory T Cells in Alleviating Aromatase Inhibitor-Induced Pain

13 mai 2026 mis à jour par: Yi Feng, MD, Peking University People's Hospital

The goal of this clinical trial is to learn whether transcutaneous auricular vagus nerve stimulation, also called taVNS, can help relieve aromatase inhibitor-related joint and muscle pain in adult women with hormone receptor-positive breast cancer.

The main questions this study aims to answer are:

  1. Does taVNS reduce pain caused by aromatase inhibitor treatment?
  2. Does taVNS improve quality of life, mood symptoms, and the need for pain medicine?
  3. What side effects or medical problems occur during treatment?

Researchers will compare active taVNS with sham stimulation. Participants in both groups will receive mild electrical stimulation around the ear, but the sham stimulation will be applied to an area not expected to activate the vagus nerve.

Participants will:

  1. Be randomly assigned to active taVNS or sham stimulation
  2. Receive one 30-minute treatment session every day for 28 days
  3. Complete pain, mood, and quality-of-life questionnaires before treatment, after treatment, and during follow-up
  4. Report pain medicine use and any side effects
  5. Provide small blood samples to measure inflammatory markers, T-cell profiles, and tumor markers

Participants will be followed for up to 6 months after treatment. For some participants who do not have enough pain relief after taVNS, an optional second-stage study may be offered. In this stage, participants may receive low-dose interleukin-2, also called IL-2, by injection every other day for 2 weeks.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

216

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

    • Beijing Municipality
      • Beijing, Beijing Municipality, Chine, 100044
        • Peking University People's Hospital
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  1. Female participants aged over 18 years;
  2. Patients with pathologically confirmed stage I-III primary breast cancer;
  3. Patients who have recovered from systemic symptoms related to surgery, radiotherapy, or chemotherapy;
  4. Patients with estrogen receptor- and/or progesterone receptor-positive breast cancer who are receiving aromatase inhibitor therapy and have aromatase inhibitor-related musculoskeletal pain, with a score greater than 3 on the Worst Pain item of the Brief Pain Inventory (BPI-WP);
  5. Patients who have received aromatase inhibitor therapy for more than 30 days and are expected to continue treatment for more than 1 year;
  6. Patients who voluntarily agree to participate in this study and sign the informed consent form.

    For participants receiving combined IL-2 treatment, the following additional criterion applies:

  7. Pain relief rate of less than 50% after taVNS treatment and a lower peripheral blood Treg count than before treatment.

Exclusion Criteria:

  1. Patients with advanced breast cancer;
  2. Patients with other significant organ dysfunction, such as major cardiovascular disease, diabetes mellitus, or hyperthyroidism;
  3. Patients with other cancers;
  4. Patients with a history of fracture or surgery around the painful joint area within the past 6 months;
  5. Patients currently receiving corticosteroids or opioid therapy;
  6. Patients with contraindications to vagus nerve stimulation;
  7. Patients who are unable to communicate normally, such as those with cognitive impairment or hearing impairment;
  8. Patients who have participated in another clinical trial within the past 1 month.

    For participants receiving combined IL-2 treatment, the following additional exclusion criteria apply:

  9. Severe cardiac or renal disease, or hematologic disease;
  10. Previous IL-2-related toxic reaction or allergy;
  11. Use of other biologic agents or immunosuppressive drugs within the past 1 month;
  12. Any other condition that the investigator considers unsuitable for study participation.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Double

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: transcutaneous auricular vagus nerve stimulation group
Electrodes will be placed on specific areas of the participant's left external ear that are mainly innervated by the auricular branch of the vagus nerve. The electrodes will be connected to an electrical stimulation device, and stimulation will be delivered at tolerable intensity using preset study parameters. Treatment will be given once daily for 28 consecutive days.
Electrodes will be placed on specific areas of the participant's left external ear that are mainly innervated by the auricular branch of the vagus nerve. The electrodes will be connected to an electrical stimulation device, and stimulation will be delivered at tolerable intensity using preset study parameters. Treatment will be given once daily for 28 consecutive days.
Autres noms:
  • taVNS
Comparateur factice: sham stimulation group
Compared with transcutaneous auricular vagus nerve stimulation group, electrodes will be placed on different areas of the participant's left external ear that are not innervated by the auricular branch of the vagus nerve. The electrodes will be connected to an electrical stimulation device, and stimulation will be delivered at tolerable intensity using preset study parameters. Treatment will be given once daily for 28 consecutive days.
Compared with transcutaneous auricular vagus nerve stimulation group, electrodes will be placed on different areas of the participant's left external ear that are not innervated by the auricular branch of the vagus nerve. The electrodes will be connected to an electrical stimulation device, and stimulation will be delivered at tolerable intensity using preset study parameters. Treatment will be given once daily for 28 consecutive days.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
The pain relief rate of patients at the end of the 4-week treatment period
Délai: From enrollment to the end of treatment at 4 weeks.
From enrollment to the end of treatment at 4 weeks.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Pain relief rate at follow-up
Délai: At 1, 2, 3, and 6 months after completion of treatment.
At 1, 2, 3, and 6 months after completion of treatment.
Dosage of analgesic drugs
Délai: At 1, 2, 3, and 6 months after completion of treatment.
At 1, 2, 3, and 6 months after completion of treatment.
Depression scores
Délai: At 1, 2, 3, and 6 months after completion of treatment.
PHQ-9 is used to measure depression. PHQ-9 ( unabbreviated scale title: Patient Health Questionnaire-9) Minimum Value: 0 Maximum Value: 27 Score Interpretation: Higher scores mean a WORSE outcome. Details:The PHQ-9 is a screening tool for depression. A higher score indicates more severe depressive symptoms. Generally, scores are interpreted as follows: 0-4 (Minimal), 5-9 (Mild), 10-14 (Moderate), 15-19 (Moderately Severe), and 20-27 (Severe) depression.
At 1, 2, 3, and 6 months after completion of treatment.
Anxiety scores
Délai: At 1, 2, 3, and 6 months after completion of treatment.
GAD-7 is used to measure anxiety. GAD-7 (unabbreviated scale title: Generalized Anxiety Disorder-7) Minimum Value: 0 Maximum Value: 21 Score Interpretation: Higher scores mean a WORSE outcome. Details:The GAD-7 measures the severity of generalized anxiety disorder. A higher score reflects more frequent and severe anxiety symptoms. Typical interpretations are: 0-4 (Minimal), 5-9 (Mild), 10-14 (Moderate), and 15-21 (Severe) anxiety.
At 1, 2, 3, and 6 months after completion of treatment.
Quality of life score
Délai: At 1, 2, 3, and 6 months after completion of treatment.

Quality of life assessed by the EuroQol 5-Dimension 5-Level questionnaire and EuroQol Visual Analogue Scale

Description:

Quality of life will be assessed using the EuroQol 5-Dimension 5-Level questionnaire (EQ-5D-5L) and the EuroQol Visual Analogue Scale (EQ VAS). For the EQ-5D-5L descriptive system, scores range from 5 to 25, with higher scores indicating worse health status. For the EQ VAS, scores range from 0 to 100, with higher scores indicating better self-rated health status.

At 1, 2, 3, and 6 months after completion of treatment.
Plasma inflammatory marker levels
Délai: Baseline, immediately after completion of treatment, and 6 months after completion of treatment.
Baseline, immediately after completion of treatment, and 6 months after completion of treatment.
The proportion of T cells in the blood
Délai: Baseline, immediately after completion of treatment, and 6 months after completion of treatment.
Baseline, immediately after completion of treatment, and 6 months after completion of treatment.
The count of T cells in the blood
Délai: Baseline, immediately after completion of treatment, and 6 months after completion of treatment.
Baseline, immediately after completion of treatment, and 6 months after completion of treatment.

Autres mesures de résultats

Mesure des résultats
Délai
Tumor marker levels
Délai: Baseline, immediately after completion of treatment, and 6 months after completion of treatment.
Baseline, immediately after completion of treatment, and 6 months after completion of treatment.
Adverse events and serious adverse events
Délai: Adverse events and serious adverse events will be recorded throughout the study.
Adverse events and serious adverse events will be recorded throughout the study.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

6 mai 2026

Achèvement primaire (Estimé)

31 décembre 2028

Achèvement de l'étude (Estimé)

31 décembre 2029

Dates d'inscription aux études

Première soumission

5 mai 2026

Première soumission répondant aux critères de contrôle qualité

13 mai 2026

Première publication (Réel)

18 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

18 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

13 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 2026PHB256-001
  • 82571385 (Autre subvention/numéro de financement: National Natural Science Foundation of China)

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

To protect patient privacy and ensure the security of clinical data, the individual participant data (IPD) collected in this study will be used only for scientific analysis and publication related to this trial. No public disclosure, sharing, or uploading to public repositories is planned. Therefore, IPD will not be made available.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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