Electroacupuncture Treatment of Peripheral Neuropathy After Taxane Chemotherapy for Breast Cancer
Recruiting now · Not applicable
Conditions studied: Breast Cancer
In brief
Electroacupuncture treatment of peripheral neuropathy after taxane chemotherapy for breast cancer
Key facts
- Study ID
- NCT06772935
- Run by
- Affiliated Hospital of Qinghai University
- People needed
- 162
- Starts
- 2025-06-01
- Expected to finish
- 2027-12-31
- Last updated by the study team
- 2025-01-14
Who can join
Age: 18 and older, up to 75. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Breast cancer patients diagnosed by pathology;
- EOOG score is 0 or 1;
- The age range for enrollment is between 18 and 75 years old; ④ Accept chemotherapy regimens based on taxane drugs (alone or in combination);
- ⑤ Previously received taxane chemotherapy for more than 6 months;
- ⑥ According to the National Cancer Institute (NCI) Common Terminology for Adverse Events (CTCAE) 5.0, reporting CIPN symptoms of grade 1 or higher for more than 2 weeks;
- ⑦ Voluntarily participate in this clinical trial and sign the informed consent form;
- Accept regular follow-up visits; ⑨ There is complete pathological data available.
You may not qualify if…
- Non breast cancer patients;
- Received electroacupuncture treatment within 6 months prior to the start of the study;
- Patients who experience intolerable toxic side effects during standard dose chemotherapy and terminate the chemotherapy cycle;
- Prior to enrollment, there was a history of peripheral neuropathy;
- Unstable heart disease or myocardial infarction within the first 6 months of the study;
- ⑥ Active skin diseases or surface skin ulcers or infections that cannot tolerate electroacupuncture treatment;
- ⑦ Uncontrolled epilepsy patients with uncontrolled seizures;
- ⑧ Merge with other malignant tumor patients;
- ⑨ Pregnancy and lactation period;
- ⑩ Refusal to join clinical trial patients
Where it is running
- Qinghai University Affiliated Hospital — Xining, Qinghai, China (enrolling)
Full record on ClinicalTrials.gov
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