Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
FEMALE
NCT06772935

Electroacupuncture Treatment of Peripheral Neuropathy After Taxane Chemotherapy for Breast Cancer

Led by Affiliated Hospital of Qinghai University · Updated on 2025-01-14

162

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Electroacupuncture treatment of peripheral neuropathy after taxane chemotherapy for breast cancer

CONDITIONS

Official Title

Electroacupuncture Treatment of Peripheral Neuropathy After Taxane Chemotherapy for Breast Cancer

Who Can Participate

Age: 18Years - 75Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Breast cancer patients diagnosed by pathology
  • EOOG score is 0 or 1
  • Age between 18 and 75 years old
  • Accept chemotherapy regimens based on taxane drugs (alone or in combination)
  • Previously received taxane chemotherapy for more than 6 months
  • Report chemotherapy-induced peripheral neuropathy symptoms of grade 1 or higher for more than 2 weeks
  • Voluntarily participate and sign informed consent
  • Accept regular follow-up visits
  • Have complete pathological data available
Not Eligible

You will not qualify if you...

  • Not diagnosed with breast cancer
  • Received electroacupuncture treatment within 6 months prior to the study
  • Experienced intolerable toxic side effects during standard dose chemotherapy causing termination
  • History of peripheral neuropathy before enrollment
  • Unstable heart disease or myocardial infarction within 6 months before the study
  • Active skin diseases, ulcers, or infections that cannot tolerate electroacupuncture
  • Uncontrolled epilepsy with seizures
  • Presence of other malignant tumors
  • Pregnancy or lactation
  • Refusal to join the clinical trial

AI-Screening

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Trial Site Locations

Total: 1 location

1

Qinghai University Affiliated Hospital

Xining, Qinghai, China, 810001

Actively Recruiting

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Research Team

G

Guoshuang Shen G Administrative Director of Breast Center, Affiliated Hospital

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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