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Clinical observation of chemotherapy induced peripheral neuropathy in patients and its correlation with traditional Chinese medicine syndrome types

Clinical observation of chemotherapy induced peripheral neuropathy in patients and its correlation with traditional Chinese medicine syndrome types

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081258
Enrollment
Unknown
Registered
2024-02-27
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Sponsors

Tianjin Cancer Hospital Airport Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Patients diagnosed with malignant tumors through pathology or cytology; 2) Age range from 18 to 80 years old, regardless of gender; 3) Expected survival time = 3 months; 4) Individuals who have developed CIPN symptoms after receiving chemotherapy with neurotoxic drugs such as platinum, paclitaxel, vinblastine, bortezomib, and thalidomide, and those with NCI grade I or above neuropathic symptoms; 5) Patients without strict center of gravity, kidney, liver, lung, or hematopoietic system dysfunction; 6) Clear consciousness, able to communicate normally, able to cooperate with medical staff to complete questionnaire surveys, physical examinations and evaluations; 7) Voluntarily participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1) Expected survival time<3 months; 2) Patients with neurological compression symptoms caused by secondary tumors caused by brain metastasis or other; 3) Patients with multiple organ failure caused by neurological disorders such as poisoning, infection, radiation therapy, or other reasons; 4) Neuropathy caused by diabetes peripheral neuropathy or other self basic diseases; 5) Individuals with severe liver and kidney dysfunction, cardiovascular and cerebrovascular diseases, or other serious complications; 6) Unsigned informed consent form; 7) Patients undergoing treatment with other drugs that may cause neurotoxicity; 8) Patients with symptomatic and difficult to control neurological, psychiatric, or psychiatric disorders.

Design outcomes

Primary

MeasureTime frame
EORTC QLQ-CIPN20 Neurotoxicity Evaluation Criteria;

Secondary

MeasureTime frame
Quality of Life score(EORTC QLQ-C30);

Countries

China

Contacts

Public ContactZhuchen Yan

Tianjin Cancer Hospital Airport Hospital

yanzc@126.com+86 186 2222 1259

Outcome results

None listed

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