Development of Complex Regional Pain Syndrome (CRPS) Severity Score As A Clinical Tool To Monitor Disease Progressio
Not Applicable
- Conditions
- Complex Regional Pain Syndrome
- Registration Number
- JPRN-UMIN000007437
- Lead Sponsor
- Department of Pain Medicine, Osaka University Graduate school of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
patients that don't meet the 2011 provisional IASP diagnostic criteria for CRPS
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measures will include the following: 1) a database sheet recording CRPS-related signs and symptoms displayed during the history and physical examination, 2) The McGill Pain Questionnaire-Short Form (MPQ-SF)6, 3) the SF-367 (with validated versions available in many languages, including Dutch, German, and Hebrew), 4) Pain and Anxiety Symptoms Scale8 (PASS-20), 5) Pain Disability Index9 (PDI), 6) Center for Epidemiologic Studies Short Depression Scale10 (CESD-10), 7) Occupational Status Questionnaire (OSQ), and 8) Patient Global Impression of Change (PGIC).
- Secondary Outcome Measures
Name Time Method