Skip to content

Application of Huangqi Guizhi Wuwu Decoction and acupuncture intervention in the prevention and treatment of taxane related peripheral neurotoxicity in patients with breast cancer: A phase II multicenter randomized controlled study

Application of Huangqi Guizhi Wuwu Decoction and acupuncture intervention in the prevention and treatment of taxane related peripheral neurotoxicity in patients with breast cancer: A phase II multicenter randomized controlled study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000623
Enrollment
Unknown
Registered
2025-04-01
Start date
2025-05-08
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Breast Cancer

Interventions

control group:Health education and clinical intervention
Test group one:Health education and Huangqi Guizhi Wuwu decoction
Test group two:Health education and acupuncture treatment

Sponsors

National Cancer Center Chinese Academy of Medical Sciences / Cancer Hospital of Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Patients with breast cancer confirmed by histology or pathology; 2) Age 18-70 years old; 3) Plan to receive or have received paclitaxel drugs: including paclitaxel docetaxel albumin Paclitaxel; 4) The estimated survival time is more than 3 months; 5) It conforms to the category of syndrome differentiation and treatment of blood stasis in traditional Chinese medicine; 6) Patients with good compliance; 7) The patient has no disturbance of consciousness and can communicate with normal language;

Exclusion criteria

Exclusion criteria: 1) Age 70 years old; 2) Peripheral neuropathy caused by other reasons; 3) There are heart liver and kidney dysfunction cardiovascular disease and endocrine disorders; Accompanied by mental and consciousness disorders; Serious skin disease and systemic infection; 4) The patient was involuntary.

Design outcomes

Primary

MeasureTime frame
Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0;European Organization for Research and Treatment of Cancer Quality of Life Questionnaire – Chemotherapy-Induced Peripheral Neuropathy Module (EORTC QLQ-CIPN20);Clinical Version of Total Neuropathy Score;

Secondary

MeasureTime frame
Psychological State Rating Scale;Syndrome Level Evaluation and Functional Index (SLEFI);European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30);

Countries

China

Contacts

Public ContactZhaoFang

National Cancer CenterChinese Academy of Medical Sciences/Cancer Hospital of Peking Union Medical College

13671045893@163.com13671045893

Outcome results

None listed

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