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

13 maggio 2026 aggiornato da: 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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

216

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Cina, 100044
        • Peking University People's Hospital
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: 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.
Altri nomi:
  • taVNS
Comparatore fittizio: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
The pain relief rate of patients at the end of the 4-week treatment period
Lasso di tempo: From enrollment to the end of treatment at 4 weeks.
From enrollment to the end of treatment at 4 weeks.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Pain relief rate at follow-up
Lasso di tempo: 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
Lasso di tempo: At 1, 2, 3, and 6 months after completion of treatment.
At 1, 2, 3, and 6 months after completion of treatment.
Depression scores
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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.

Altre misure di risultato

Misura del risultato
Lasso di tempo
Tumor marker levels
Lasso di tempo: 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
Lasso di tempo: Adverse events and serious adverse events will be recorded throughout the study.
Adverse events and serious adverse events will be recorded throughout the study.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

6 maggio 2026

Completamento primario (Stimato)

31 dicembre 2028

Completamento dello studio (Stimato)

31 dicembre 2029

Date di iscrizione allo studio

Primo inviato

5 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

13 maggio 2026

Primo Inserito (Effettivo)

18 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

13 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2026PHB256-001
  • 82571385 (Altro numero di sovvenzione/finanziamento: National Natural Science Foundation of China)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano 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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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