Clinical Research Directory

Inclusion Criteria: The study will enroll patients with a symptom of peripheral neuropathy, including paresthesia, numbness, glove-and-stocking sensory loss distribution or pain in four limbs, and meet the following inclusion criteria: 1. All adult cancer patients (Age≧20-year-old) who received chemotherapy regimens, including adjuvant and neoadjuvant therapy 2. Stage I-III cancer patients 3. Completed chemotherapy regimens more than3 months, including Taxanes (paclitaxel or docetaxel), platinum (cisplatin, oxaliplatin, carboplatin) 4. Baseline von Frey Monofilament test (Target force at hand) ≧ 0.07gms 5. Baseline von Frey Monofilament test (Target force at foot) ≧ 0.4gms 6. Eastern Cooperative Oncology Group (ECOG) performance status ≦3 7. Grading of peripheral sensory neuropathy in National Cancer Institute- common terminology criteria for adverse events,v5.0 (NCI-CTCAE5) ≧1 8. Patients were restricted acupuncture treatment for one month before recruitment 9. Written patient informed consent Exclusion Criteria: Participants with any of the following conditions will be excluded: 1. Uncontrolled Diabetic Mellitus, HbA1c≧7% is inappropriate\[19\]. 2. Diabetic neuropathy diagnosed before receiving chemotherapy 3. Neuropathy from any type of nerve compression (e.g., carpal/tarsal tunnel syndrome, radiculopathy, spinal stenosis, brachial plexopathy) 4. Concomitant with duloxetine, or another analgesia, including Pregabalin, Venlafaxine, Minocycline, Topical gel, Oxycodone, Naloxone, Cannabinoids, and Angiotensin II type 2 receptor antagonist 5. Severe hemorrhagic coagulopathy or bleeding tendency 6. Unstable cardiovascular disease 7. Severe skin lesions around the treatment sites The researchers will exclude any participants considered to be inappropriate for the study.