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Integrated Chinese and Western Medicine Rehabilitation Management for Chemotherapy-Induced Peripheral Neuropathy: A Randomized Controlled Trial

Integrated Chinese and Western Medicine Rehabilitation Management for Chemotherapy-Induced Peripheral Neuropathy: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124576
Enrollment
Unknown
Registered
2026-05-14
Start date
2026-01-10
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Chemotherapy-Induced Peripheral Neuropathy

Interventions

Group A :TCM fumigation therapy plus Sensorimotor Training
Group B:TCM fumigation therapy
Group C:Mecobalamin Treatment

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with a histopathological diagnosis of cancer who are receiving chemotherapy regimens that may induce chemotherapy-induced peripheral neuropathy (CIPN), such as taxanes or platinum-based agents; (1)Patients who meet the above Western medicine diagnostic criteria as well as the Traditional Chinese Medicine (TCM) syndrome differentiation criteria for "Yang deficiency and cold coagulation"; 2. Age between 18 and 70 years; 3. No symptoms of CIPN (such as numbness, tingling, or hypoesthesia) prior to chemotherapy administration; 4. No severe systemic diseases, including: (1)Cardiovascular system: congestive heart failure (NYHA class III–IV), acute myocardial infarction, or uncontrolled hypertension (>180/110 mmHg); (2)Respiratory system: acute exacerbation of moderate-to-severe chronic obstructive pulmonary disease (COPD) or severe asthma; (3)Hepatic and renal function: severe hepatic failure (Child–Pugh class C) or renal failure (eGFR <30 mL/min); (4)Hematologic system: severe anemia (Hb <70 g/L) or platelet count <50×10^9/L; 5. Patients who voluntarily agree to participate in the study, sign the informed consent form, and are able to complete follow-up assessments as required.

Exclusion criteria

Exclusion criteria: 1. preexisting peripheral neuropathy due to other causes: neurological injury due to other neurological disorders (such as diabetic neuropathy, myelopathy, post-traumatic sequelae, etc.) ; 2. cognitive impairment or mental illness, inability to complete research interventions or assessments (EG, severe dementia, schizophrenia) ; 3. allergic to any of the pharmaceutical ingredients in the fumigated washing formula; 4. presence of skin infection, wound or other serious skin condition.

Design outcomes

Primary

MeasureTime frame
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Chemotherapy-Induced Peripheral Neuropathy 20-item scale( EORTC QLQ-CIPN20));

Secondary

MeasureTime frame
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core Scale(EORTC QLQ-C30);

Countries

China

Contacts

Public ContactXiaonan Cui

The First Affiliated Hospital of Dalian Medical University

cxn23@sina.com+86 180 9887 6725

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026