Evaluation of pain characteristics and pain course after surgical reconstruction of scaphoid pseudarthrosis
Recruiting
- Conditions
- M84.14F45.41
- Registration Number
- DRKS00025302
- Lead Sponsor
- BG KLinik Ludwigshafen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Target group of this study are patients for which a surgical reconstruction of scaphoidpseudarthrosis is planned. The decision for the inclusion citeria of a patient of this study are independent of the genesis (posttrauamtic, infect, etc.) of the pseudarthrosis and the planned operation technique (cancellous bone, iliac crest, pedicled or free vascularised bone grafts). The selection of the patients is independent of sex and previous illnesses. A further inclusion criterion is the patient’s written informed consent.
Exclusion Criteria
Exclusion citeria are the participation in another study as well as patient‘s age (under 18 or over 65). Withdrawel of the informed consent leads also to an exclusion of the study.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary aim of this project is the identification of preoperative existing reaction patterns to pain stimuli, other sensoric stimuli and psychosocial risk factors that could explain different pain progressions after surgical reconstruction of the scaphoidpseudarthrosis.
- Secondary Outcome Measures
Name Time Method Hand function after surgical reconstruction of the scaphoidpseudarthrosis