Neuropathic pain induced by chemotherapy for breast and gynecological cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with peripheral neuropathic pain induced by chemotheraphy for breast or gynecological cancer Patients with pain duration of 3 months or longer Patients with moderate or sevvere pain (VAS: 30mm or more) Patients with agreement with no change of ordinary drugs during trial Patients with an informed consent given
Exclusion criteria
Exclusion criteria: Patients suffering from cognitive impairments, aphasia, or a major psychiatric disease Patients with a desire for suicide Patients who cannot write the questionnaires Patients with an implanted metal in a head excluding a mouth Patients with a cardiac pacemaker, devices for deep brain stimulation, or an implanted medication pump Patients suffering from serious heart diseases Patients suffering from a major cerebral infarction or head a trauma Patients suffering from a brain tumor Patients with epilepsy episode history Pregnant patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain reduction in visual analogue scale | — |
Countries
Japan
Contacts
Osaka University Department of Neuromodulation and Neurosurgery