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Clinical study of precision moxibustion of twelve well points in patients with peripheral neuropathy associated with paclitaxel chemotherapy in gynecology

Clinical study of precision moxibustion of twelve well points in patients with peripheral neuropathy associated with paclitaxel chemotherapy in gynecology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066683
Enrollment
Unknown
Registered
2022-12-13
Start date
2022-12-19
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

paclitaxel chemotherapy induced peripheralneuropathy

Interventions

Treatment group:Precision Moxibustion Twelve Well Points+Mecobalamin

Sponsors

The Second Clinical College,Guangzhou University of Chinese Medicine University-town Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age 20-70 years old. (2) Patients with pathologically confirmed gynecologic malignancies treated with paclitaxel alone (including regular paclitaxel, paclitaxel liposome, and albumin paclitaxel) or in combination with chemotherapy. (3) After receiving at least one course of paclitaxel chemotherapy and developing symptoms of peripheral neuropathy. (4) No serious cardiac, hepatic or renal disorders and no history of diabetes. (5) No local skin breakdown. (6) Sign the informed consent form, voluntarily accept the treatment of this protocol, and adhere to and cooperate with the treatment during the observation cycle.

Exclusion criteria

Exclusion criteria: (1) Combination of peripheral neuropathy due to acute or post-acute phase of cerebrovascular disease, alcohol dependence, diabetes, malnutrition, and hypothyroidism. (2) Combined cellulitis and venous thrombosis in the extremities. (3) Infected and broken skin on the extremities. (4) Patients currently enrolled or enrolled in another clinical trial within 1 month prior to this study.

Design outcomes

Primary

MeasureTime frame
Total Neuropathy Score;

Secondary

MeasureTime frame
The European O-rganization for Reasearch and Treatment of Cancer-Quality of Life Questionnare-Core 30;Functional Assessment of Cancer Therapy-Gynecologic Oncology Group-Neurotoxicity;

Countries

China

Contacts

Public ContactCai Lin-er

The Second Clinical College,Guangzhou University of Chinese Medicine University-town Hospital

278379980@qq.com+86 15820295788

Outcome results

None listed

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