Congenital transverse failure
Conditions
Interventions
For patients with congenital transverse failure, individualized prostheses will be fabricated and fitted according to each case. Functional evaluations will be performed during the initial period afte
Sponsors
National Center for Child Health and Development
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients diagnosed with congenital transverse failure (including transradial and transhumeral deficiencies) who provide written informed consent for participation in this study.
Exclusion criteria
Exclusion criteria: Patients with intellectual or developmental disabilities, as well as those deemed unsuitable for participation at the discretion of the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional assessment performed every six months after myoelectric prosthesis applying (number of blocks transferred in the Box and Block Test) | — |
Countries
Japan
Contacts
Public ContactTakehiko Takagi
National Center for Child Health and Development Division of Orthopaedic Surgery
Outcome results
None listed