Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

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

13 de maio de 2026 atualizado por: 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.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

216

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100044
        • Peking University People's Hospital
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: 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.
Outros nomes:
  • taVNS
Comparador Falso: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
The pain relief rate of patients at the end of the 4-week treatment period
Prazo: From enrollment to the end of treatment at 4 weeks.
From enrollment to the end of treatment at 4 weeks.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Pain relief rate at follow-up
Prazo: 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
Prazo: At 1, 2, 3, and 6 months after completion of treatment.
At 1, 2, 3, and 6 months after completion of treatment.
Depression scores
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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.

Outras medidas de resultado

Medida de resultado
Prazo
Tumor marker levels
Prazo: 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
Prazo: Adverse events and serious adverse events will be recorded throughout the study.
Adverse events and serious adverse events will be recorded throughout the study.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

6 de maio de 2026

Conclusão Primária (Estimado)

31 de dezembro de 2028

Conclusão do estudo (Estimado)

31 de dezembro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

5 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

13 de maio de 2026

Primeira postagem (Real)

18 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

18 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

13 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2026PHB256-001
  • 82571385 (Número de outro subsídio/financiamento: National Natural Science Foundation of China)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano 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.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever