Clinical response to intravenous immunoglobulin inpatients with complex regional pain syndrome (CRPS)
Completed
- Conditions
- Complex regional pain syndrome (CRPS)Signs and Symptoms
- Registration Number
- ISRCTN63918259
- Lead Sponsor
- Record Provided by the NHSTCT Register - 2006 Update - Department of Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 16
Inclusion Criteria
1. 16 patients from Pain Management aged 16 years and older, male and female
2. CRPS of between 6 and 30 months duration
3. Numeric rating scale pain score greater than 4
Exclusion Criteria
1. Pregnant or lactating women
2. IgA deficiency
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The average numeric rating scale pain value from day four to day 18 after infusions compared between IVIG and saline<br>
- Secondary Outcome Measures
Name Time Method 1. The number of patients who found either treatment more effective<br>2. The global impression of change values between day four to day 18 after infusions compared between IVIG and saline