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Clinical efficacy evaluation and mechanism study of "Tongluo Fujin" acupuncture treatment for chemotherapy related peripheral neuropathy in malignant tumors

Evaluation of Clinical Efficacy and Mechanism Study of the 'Tongluo Fujin' Acupuncture Method in Treating Chemotherapy-Induced Peripheral Neuropathy in Patients with Malignant Tumors.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002196
Enrollment
Unknown
Registered
2025-11-17
Start date
2025-01-15
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chemotherapy-induced peripheral neuropathy

Interventions

2. Fake electroacupuncture group :The sham electroacupuncture group opened 1 inch horizontally to the radial side at the acupoints of Waiguan, Quchi, Fenglong, Hegu, and Yanglingquan on both sides
The midpoint of the horizontal line connecting the bilateral Sanyin intersection and Achilles tendon. Use a 1.5-inch microneedle to lightly pierce the skin without detachment, without manual operation
3. Tongluo Fujin (TLFJ) group:The TLFJ group received the Tongluo Fujin acupuncture method, with the main acupoints selected as Waiguan, Quchi, Hegu, Yanglingquan, Fenglong, and Sanyinjiao. Using a 1.
1. Western medicine group :The Western medicine group was given oral methylcobalamin tablets three times a day 0.5 mg each time with a 7-day cycle for two consecutive cycles

Sponsors

First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with multiple myeloma, breast cancer, or colorectal cancer (regardless of type and stage); Have received at least one course of treatment with bortezomib, albumin-bound paclitaxel, or oxaliplatin; Diagnosed with PN within 6 months, presenting with numbness, reduced sensation, pain, or sensory abnormalities in the extremities; some patients may experience muscle spasms, muscle weakness, myalgia, or even paralysis; Aged over 18 years, with an expected survival period of more than 3 months; Karnofsky Performance Status (KPS) score = 60; Voluntarily agree to participate in this study, willing to undergo acupuncture treatment, and able to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with pre-existing neurological, musculoskeletal disorders, peripheral sensory abnormalities in diabetic patients, poisoning, infection, radiotherapy, or other causes of peripheral neuropathy, as well as those undergoing treatment with other drugs that may cause neurotoxicity; 2. Patients with infections or other lesions at the acupuncture site that make acupuncture therapy inadvisable; 3. Patients with platelet count (PLT) < 30×109/L prior to treatment; 4. Patients with severe cardiovascular diseases, infections, or dysfunction of the liver, kidneys, or other organs, or those with a history of needle fainting; 5. Patients with mental abnormalities, pregnant women, or breastfeeding mothers; 6. Patients currently participating in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Electroencephalogram;Grading of Peripheral Neuropathy;PNQ Rating;FACT-NTX Score;Karnofsky Performance Status;TCM syndrome score;

Secondary

MeasureTime frame
Blood Routine;Four coagulation tests;

Countries

China

Contacts

Public ContactShi Zhexin

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

shzhx0604@163.com+86 132 5268 9966

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026