A prospective observational study to evaluate the impact of neuropathic pain components on pain response to radiotherapy for painful tumors
Not Applicable
Recruiting
- Conditions
- Painful tumors
- Registration Number
- JPRN-UMIN000029579
- Lead Sponsor
- Kumamoto University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 250
Inclusion Criteria
Not provided
Exclusion Criteria
1. Some other tumor has more severe pain than the tumor planned to receive radiotherapy 2. Painful tumor planned to receive radiotherapy was previously irradiated
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain response within three months after the start of radiotherapy
- Secondary Outcome Measures
Name Time Method Pain intensity, Analgesic use, Functional interference, Performance status, Adverse events, Other painful lesions