PEPT versus CBO-therapie bij patiënten met CRPS-I/PD.
Completed
- Conditions
- CRPS IComplex Regional Pain Syndrome Type ISympathetic Reflex DystrophyPain Exposure Physical TherapyPharmacological treatmentFunctional recoveryPosttraumatische Dystrofie
- Registration Number
- NL-OMON23780
- Lead Sponsor
- Radboud University Nijmegen Medical Centre, The NetherlandsDpt. of Surgery
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 75
Inclusion Criteria
Patients between 18 and 80 years of age with Complex Regional pain Syndrome (CRPS-1) of either upper or lower extremity according to Bruehl's/IASP criteria between 3 and 24 months after initial injury will be selected for the study.
Exclusion Criteria
Patients who do not comply with the inclusion criteria, especially those who have other causes that may explain a pain syndrome will be excluded (IASP criterium).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method