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The sIL-2R level in patients referred with a suspicion of Complex Regional Pain Syndrome. Comparison between those who are diagnosed with CRPS and those who are not.

Recruiting
Conditions
Complex Regionaal Pijn Syndroom.
Reflex Sympathetic Dystrophy
Sudeck's Atrophy
Registration Number
NL-OMON44506
Lead Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
52
Inclusion Criteria

Patients who are referred to the Center for Pain Medicine with a suspicion of CRPS.
Age * 18 years.
Only one limb is affected.

Exclusion Criteria

History of an auto-inflammatory or autoimmune disease.
Current treatment with immunomodulating medication or treatment within the last 6 months.
Ill at the time of visit or recently been ill in the past two weeks.
Knowledge of or confirmed pregnancy.

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main study parameter is the blood sIL-2R level between patients diagnosed<br /><br>with CRPS and the patients who are not diagnosed with CRPS. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Association between the sIL-2R level and CRPS severity score. </p><br>
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