Correlation Between 3 Phase Bone Scintigraphy and Pressure Pain Thresholds in Patients With Complex Regional Pain Syndrome (CRPS)
NCT ID: NCT01623141
Last Updated: 2012-06-19
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
53 participants
OBSERVATIONAL
2010-10-31
2011-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Patients with CRPS
18 patients with unilateral CPRS of the upper limb were included to the study
Pressure Pain measurement
The pressure pain thresholds were established using a manual pressure algometer. The investigated joints were the carpus, the metacarpophalangeal and the proximal interphalangeal joints
Patients with limb pain of other origin
17 patients with unilateral upper limb pain of other origin served as control group
Pressure Pain measurement
The pressure pain thresholds were established using a manual pressure algometer. The investigated joints were the carpus, the metacarpophalangeal and the proximal interphalangeal joints
Healthy subjects
18 healthy subjects were included to establish reference data for the pressure pain thresholds
Pressure Pain measurement
The pressure pain thresholds were established using a manual pressure algometer. The investigated joints were the carpus, the metacarpophalangeal and the proximal interphalangeal joints
Interventions
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Pressure Pain measurement
The pressure pain thresholds were established using a manual pressure algometer. The investigated joints were the carpus, the metacarpophalangeal and the proximal interphalangeal joints
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* aged \> 18 years with written informed consent
* adequate understanding of the german language
* indication for a TPBS independent of the study
Patients with CRPS:
* patients with CRPS type 1 of the upper limb diagnosed on the basis of the budapest criteria (Harden, Bruehl et al., 2010)
* unilateral pain
Control group:
* patients with pain of the upper limbs of other origin than CRPS who underwent a TPBS
* unilateral pain
Healthy subjects:
* checked by the DFNS IMI questionnaire
Exclusion Criteria
* inadequate understanding of the german language
* disease duration of more than 12 months
* other disease of the upper extremity (e.g. polyarthrosis, rheumatoid arthritis)
* pregnancy/ lactation period
18 Years
ALL
Yes
Sponsors
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Ruhr University of Bochum
OTHER
Responsible Party
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Christoph Maier
Prof. Dr. med. (Head of the pain clinic of the Bergmannsheil University Hospital)
Principal Investigators
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Christoph Maier, Prof. Dr.
Role: STUDY_DIRECTOR
Head of the pain clinic of the Bergmannsheil University Hospital
Locations
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Bergmannsheil, department for pain management
Bochum, North Rhine-Westphalia, Germany
Countries
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Other Identifiers
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Scinti/PressurePain2011
Identifier Type: -
Identifier Source: org_study_id
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