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Efficacy of Acupuncture in Prevention of Chemotherapy Induced Peripheral Neuropathy - a Pilot Study

T

Tzu-Liang Chen

Status and phase

Unknown
Phase 3

Conditions

Colorectal Cancer

Treatments

Other: Verum acupuncture

Study type

Interventional

Funder types

Other

Identifiers

NCT02744274
CMUH104-REC1-076

Details and patient eligibility

About

The aim of this pilot study is to investigate the efficacy of acupuncture in prevention of chemotherapy induced peripheral neuropathy. The study adapted a single center, randomized, assessor- and participant-blinded, controlled, and parallel-design approach to investigate whether acupuncture can prevent or postpone the occurrence of peripheral neuropathy and improve quality of life.

Full description

Background and purpose:

Chemotherapy-induced peripheral neuropathy (CIPN) is a disabling side effect of several commonly used antineoplastic agents. CIPN prevalence was 68.1% within the first month of the end of chemotherapy, 60% at 3 months, and 30.0% at 6 months or later. Oxaliplatin as a chemotherapeutic drug for colorectal cancer has neurotoxicity on peripheral nerve system. A definite portion of patients suffered neurologic symptoms including paresthesia, dysesthesia over limbs and perioral area accompanied with muscles cramps or spasm sometimes; however, had impact on quality of life, daily functions, quality of sleep and lead to distress and depression. There is no drug to prevent peripheral neuropathy. Clinical observations reveal that acupuncture could decrease peripheral neuropathy, improve quality of life, and promote motivation of complete chemotherapy course.

Material and methods:

A total of 32 volunteers of patients with colorectal cancer will be recruited from the Chinese medicine or Western medicine clinics in China Medical University Hospital. These patients will be randomized to receive verum acupuncture or sham acupuncture treatment two times biweekly, prior to beginning chemotherapy and the weeks that drugs administered, for 26 treatments in total.

Questionnaires, neurological examination and Von Frey Filament Test will be completed at baseline, 12 and 24 weeks after initiation of intervention, 12 and 24 weeks after completion of acupuncture completion.

Predict results:

Investigators expect that the efficacy of verum acupuncture is superior to sham acupuncture in prevent or postpone occurrence of chemotherapy induced peripheral neuropathy and able to improve numbness, paresthesia, quality of life. The effectiveness of acupuncture can be detected by questionnaires, Von Frey Filament Test and neurological testing.

Enrollment

32 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients were diagnosed as stage 3 colorectal cancer.
  2. Patients are going to receive Oxaliplatin based chemotherapy.
  3. Patients are willing to cooperate with physicians and completely receive chemotherapy.
  4. Patients are willing to receive acupuncture treatments and follow-up assessments.
  5. Adult volunteers with the ages of 20-70 years old.
  6. ECOG Performance Status of 0, 1, or 2

Exclusion criteria

  1. Current active treatments with chemotherapy, radiotherapy or tumor resection surgery in the past one month.
  2. Having chemotherapy with neuropathic agents including taxane, platinum, vinca alkaloid, bortezimab, or thalidomide in the past six months.
  3. Local infection at or near the acupuncture site is not suitable for acupuncture after physician examination.
  4. Concurrent use of other alternative medicines such as herbal agents, high dose vitamins and minerals.
  5. Known coagulopathy or taking anticoagulants.
  6. Platelets < 50000/ul.
  7. WBCs < 3000/ul.
  8. Active CNS disease
  9. Cardiac pacemaker.
  10. Psychological or behavior disorder such as Schizophrenia.
  11. Currently pregnant or breastfeeding women.
  12. History of diabetic neuropathy or neuropathy related to HIV.
  13. Previous acupuncture treatment for any indication within 30 days of enrollment.
  14. Current medications that could affect symptoms related to CIPN.
  15. Grade III lymphedema or more severe situation

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

32 participants in 2 patient groups, including a placebo group

Verum acupuncture
Experimental group
Description:
16 patients will be randomized to receive verum acupuncture two times biweekly, prior to beginning chemotherapy and the weeks that drugs administered, for 26 treatments in total.
Treatment:
Other: Verum acupuncture
Sham acupuncture
Placebo Comparator group
Description:
16 patients will be randomized to receive sham acupuncture two times biweekly, prior to beginning chemotherapy and the weeks that drugs administered, for 26 treatments in total.
Treatment:
Other: Verum acupuncture

Trial contacts and locations

1

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Central trial contact

Ming-Cheng Huang, M.D; Tzu-Liang Chen, M.D., MS.

Data sourced from clinicaltrials.gov

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