Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

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

13. mai 2026 oppdatert av: 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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

216

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

    • Beijing Municipality
      • Beijing, Beijing Municipality, Kina, 100044
        • Peking University People's Hospital
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: 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.
Andre navn:
  • taVNS
Sham-komparator: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
The pain relief rate of patients at the end of the 4-week treatment period
Tidsramme: From enrollment to the end of treatment at 4 weeks.
From enrollment to the end of treatment at 4 weeks.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Pain relief rate at follow-up
Tidsramme: 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
Tidsramme: At 1, 2, 3, and 6 months after completion of treatment.
At 1, 2, 3, and 6 months after completion of treatment.
Depression scores
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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.

Andre resultatmål

Resultatmål
Tidsramme
Tumor marker levels
Tidsramme: 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
Tidsramme: Adverse events and serious adverse events will be recorded throughout the study.
Adverse events and serious adverse events will be recorded throughout the study.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

6. mai 2026

Primær fullføring (Antatt)

31. desember 2028

Studiet fullført (Antatt)

31. desember 2029

Datoer for studieregistrering

Først innsendt

5. mai 2026

Først innsendt som oppfylte QC-kriteriene

13. mai 2026

Først lagt ut (Faktiske)

18. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

18. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

13. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 2026PHB256-001
  • 82571385 (Annet stipend/finansieringsnummer: National Natural Science Foundation of China)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere