Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
40 participants
OBSERVATIONAL
2007-04-30
2008-01-31
Brief Summary
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Detailed Description
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Secondary outcome parameters: Peripheral sensory and autonomic function.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Pain in arm or hand \> 3 months.
* Diagnosed with CRPS acc. to diagnostic research criteria (Harder et al., 2005)
* Inclusion of healthy subjects: age-, gender-, and BMI-matched.
Exclusion Criteria
* Treatment with anticholinergics, sympathomimetics and parasympathomimetics, and alpha- and beta-adrenergics.
18 Years
ALL
Yes
Sponsors
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Danish Pain Research Center
OTHER
Principal Investigators
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Troels S Jensen, MD, DMSc
Role: STUDY_CHAIR
Danish Pain Research Center, Aarhus University Hospital
Locations
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Danish Pain Research Center, Aarhus University Hospital
Aarhus, , Denmark
Countries
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Other Identifiers
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Capsaicin in CRPS
Identifier Type: -
Identifier Source: org_study_id
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