chirurgische verrichtingen t.b.v. oncologische aandoeningen of trauma above knee amputation, transfemoral amputation above the knee amputation
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - The participant has a primary unilateral transfemoral amputation; - The transfemoral amputation was performed 1 to 15 years ago; - The participant is aged >= 18 years; - The participant is fitted with a prosthesis and is using it; - The participant meets the criteria to be eligible for an MRI, which will be confirmed by checking the 'Screeningsformulier MRI-onderzoek'
Exclusion criteria
Exclusion criteria: - The participant is unwell or is showing signs of dementia, limiting reading the information letter and filling in the screening form; - The participant does not have sufficient knowledge of the Dutch language to read the information letter or answer the questions; - Participants with a bone-anchored prothesis; - Participants with a bilateral amputation; - Participants with an implant; - Participants who have a contraindication for MRI after screening.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary study parameters are the muscle volume (cm3) of the adductors, abductors, flexors and extensors of the hip, the amount of intermuscular fat (cm3), and the hip muscle strength. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study parameters include the femur length and the score on the mobility test (L-Test). | — |
Countries
Netherlands
Contacts
Universitair Medisch Centrum Groningen