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Clinical Trial Summary

The present study aims to evaluate the effectiveness of acupuncture in the treatment of chemotherapy drug paclitaxel induced peripheral neuropathy in patients with early stage breast cancer


Clinical Trial Description

Patients with early stage breast cancer (stages I,II,III) who received paclitaxel in neoadjuvant or adjuvant chemotherapy protocol and developed peripheral neuropathy will be randomized to receive true acupuncture (intervention group) vs sham acupuncture (control), once a week, for 8 weeks. The primary outcome is improvement of the symptoms by Neuropathic Pain Symptom Inventory (NPSI) scale (Bouhassira,2004). The secondary outcomes are improvements on Visual analog scale (VAS) and Quality of life by FACT-taxane (Cella, 2003) questionnaire. These scales will be assessed in the Screening visit (baseline), week 4, week 6, week 8 and week 12. The study has duration of 12 weeks. ;


Study Design


Related Conditions & MeSH terms

  • Peripheral Nervous System Diseases
  • Peripheral Neuropathy Due to Chemotherapy

NCT number NCT04461977
Study type Interventional
Source Instituto Brasileiro de Controle do Cancer
Contact
Status Completed
Phase N/A
Start date January 30, 2020
Completion date March 26, 2024

See also
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Recruiting NCT03571334 - Botulinum Toxin A for the Treatment of Chemotherapy Induced Peripheral Neuropathy Phase 2
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