M84.14 F45.41
Conditions
Interventions
Group 1: PreOp:
- Health history, occupational history, social history.
Preop and 6 months postop:
- Bony consolidation (radiographic and CT findings independent of study).
- Hand function (extension
Sponsors
BG KLinik Ludwigshafen
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
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 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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Hand function after surgical reconstruction of the scaphoidpseudarthrosis | — |
Countries
Germany
Contacts
Public ContactVictoria Struckmann
BG Klinik LudwigshafenKlinik für Hand, Plastische und Rekonstruktive Chirurgie – SchwerbrandverletztenzentrumKlinik für Hand und Plastische Chirurgie an der Universität Heidelberg
Outcome results
None listed