An Investigation Into a New Manufacture Technique of Trans-femoral Sockets

The test will be a single group prospective pre/post design. Amputees are a small proportion of the general population. The population group specified in the inclusion/exclusion criteria is a further subsample of amputees. For practical reasons, i.e. to achieve statistical power, it is therefore more feasible to use within-subject comparison rather than creating study arms to compare. Furthermore, as mobile amputees generally have and use a prosthetic device for their daily activities, within-comparison is feasible comparing to the subjects' previous device. All investigational activities will be conducted at prosthetic out-patient clinics. As stated above the primary endpoint is successful use rate, see Table 2, and the secondary endpoints are listed in the table from B-H in that respective order of significance. See previous chapter on objectives and hypothesis and Table 2 for rationale. Drop-outs and withdrawals will not be replaced. Equipment required for each subject: * Pen/pencil * Printed out instruments * Investigational device: Materials for making DS-TF socket o Designated locking or seal-in liner to be fitted with the socket Additionally, each LPI or LCI will have access to: * Equipment for DS-TF socket manufacturing * iPad with the Össur ProApp installed for data collection The equipment used does not require specific monitoring, maintenance or calibration procedures. The purpose of the study is to evaluate in a cohort the time it takes to manufacture and delivery (lead time) of a definitive prosthesis (definition of finished prosthetic leg is, a prosthesis that is individually tailored and able to be used both indoors and outdoors, with the maximum weight on the patient equivalent to 160 kg). The existing prosthesis is to be evaluated as well as the new socket. The evaluation of function will take place at baseline, 6 weeks and 6 months after deliverance. The following outcome instruments will be used: • At all three study evaluation points; initial fitting, 6 wees and 6 months: * OPUS (LEFS, CSD, CSS) https://www.sralab.org/rehabilitation-measures/orthotics-prosthetics-users-survey * ProAMP (to test the current function with prosthesis) * EQ-5D (for life quality) * Socket Comfort Score (SCS) * CLASS - socket fit * Plus-M * ABC * TUG Cost of fitting, to all parties, will be collected and reported. Whatever the outcome of the study will be, it will be very informative for healthcare systems, both payers and providers, and manufacturer of equipment for amputees. The total time required to implement the full clinical investigation is expected to be approximately 26 months. Each individual subject is expected to participate in the clinical investigation for a minimum of 6 weeks, up to 6 months. The estimated time needed to include the required number (enrolment period) is 20 months.