Amputatie onderste extremiteit Lower limb amputation transtibial amputation
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Recently amputated patients. Patients admitted to the University Medical Centre Groningen or the Martini Hospital in Groningen. Patients with the intention to use a prosthesis. Patients who agreed to participate and gave informed consent. An adequate state of health to undergo the measurements. Patients who are at least 18 years of age and who are legitimately capacitated
Exclusion criteria
Exclusion criteria: Patients who won*t be able to use a prosthesis. Patients who didn*t give informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main study parameters/ endpoints: • Stump volume • Time until a stable stumpvolume has been reached • Variability in stump volume | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study parameters/ endpoints: • Age • Sex • Illness which has been the cause of the need to amputate • Co-morbidity • Post-operative wound dressing (bandaging, plaster cast, liners, etc.) • Activity level (pre- en postoperative) • Time of day when taking the measurement | — |
Countries
Netherlands