Patients who developed peripheral neuropathy during chemotherapy treatment at our hospital and were evaluated as NCI-CTCEA Grade 2 by the pharmacist
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients 18 years of age or older who have been evaluated as Grade 2 or higher by the chemotherapy room pharmacist between the date of approval and December 31, 2028. Patients who have given written consent to participate in this study
Exclusion criteria
Exclusion criteria: Patients being treated with implantable medical devices such as pacemakers and ICDs Other patients who are judged to be inappropriate by the doctor's judgment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| [Main evaluation items] Patient VAS and questionnaire method FACT/GOG-Ntx (Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity), PNQ (Patient Neurotoxicity Questionnaire) and Pain vision (pain frequency, lowest perceived current value, pain perceived current value ) [Secondary evaluation items] participation rate Effectiveness of supportive care (duloxetine, gabapentinoids, opioids) | — |
Countries
Japan
Contacts
Gifu University Hospital Department of Anesthesiology and Pain Medicine