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Comprehensive Fire-dragon Cupping Moxibustion for Axillary Web Syndrome in Patients After Breast Cancer Surgery: A Randomized Controlled Trial of Efficacy and Safety

Efficacy and Safety of Comprehensive Fire-dragon Cupping Moxibustion for Axillary Web Syndrome in Patients After Breast Cancer Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001710
Enrollment
Unknown
Registered
2026-07-09
Start date
2026-07-13
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Axillary Web Syndrome in Patients After Breast Cancer Surgery

Interventions

Experimental Group:Comprehensive Fire-dragon Cupping Moxibustion was administered to the experimental group on the basis of routine nursing care.

Sponsors

Guangdong Women and Children Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients who have previously undergone breast cancer surgery and have been clinically diagnosed with axillary web syndrome by a specialist. (2) Patients who have experienced their first occurrence of axillary nerve syndrome and have not undergone any intervention. (3) Patients who are able to cooperate in completing the relevant scales and examinations. (4) There are no other lesions or surgical interventions in the axilla, shoulder, or hand areas. (5) Patients voluntarily participate in this study and sign the informed consent form. (6) Age = 18 years and = 65 years.

Exclusion criteria

Exclusion criteria: (1)Advanced Breast Cancer (2) Presence of distant metastasis (3) In cases involving major diseases affecting other organs, abnormal cognitive or behavioral conditions, or other limitations on activities. (4) Patients with heat syndrome: Those diagnosed with genuine heat syndrome or yin deficiency with excessive fire syndrome according to traditional Chinese medicine. (5) Patients allergic to mugwort, wool, or massage oil (6) Patients participating simultaneously in other studies due to axillary nerve syndrome. (7) Skin damage, ulcers, infections, or active dermatitis on the affected side of the upper limb. (8) History of radiation exposure to the affected axillary fossa and upper limb area. (9) Patients diagnosed with moderate lymphedema in the affected upper limb.

Design outcomes

Primary

MeasureTime frame
University of California, Los Angeles Shoulder Rating Scale;

Secondary

MeasureTime frame
Visual Analogue Scale (VAS) for pain;Shoulder range of motion includes forward flexion, extension, abduction, and horizontal abduction.;European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30;

Countries

China

Contacts

Public ContactHuang Tang

Guangdong Women and Children Hospital

syx1230214@163.com15920853720

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026