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QUANTIFYING PROSTHESIS ALIGNMENT IN TRANSTIBIAL BONE-ANCHORED PROSTHESIS USERS

QUANTIFYING PROSTHESIS ALIGNMENT IN TRANSTIBIAL BONE-ANCHORED PROSTHESIS USERS - Optimizing BAP Alignment

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON52260
Enrollment
27
Registered
2022-05-17
Start date
2022-06-23
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bot-verankerde prothesegebruikers bone-anchored prosthesis Osseointergration

Interventions

None listed

Sponsors

Radboudumc Nijmegen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Persons will be eligible for the study if they use a unilateral trans-tibial bone-anchored prosthesis for at least one year. They need to be able to walk without additional assistive devices during the measurements. An activity level of K3-K4 is required and all participants should be over 18 years of age.

Exclusion criteria

Exclusion criteria: Persons with cognitive or communicative limitations or visual limitations as well as physical co-morbidity, that would hinder smooth locomotion and save locomotion during the measurements, will be excluded from participation in this study .

Design outcomes

Primary

MeasureTime frame
The level of symmetry in moments around the hip and knee between the residual limb and the sound limb. This data will be collected at self-selected comfortable walking speed, and we will compare baseline alignment condition to the WBL alignment condition within the participants.

Secondary

MeasureTime frame
Investigating the relationship between a structural change in alignment and the change in knee, hip and implant moments in trans-tibial bone-anchored prosthetic users in the frontal plane. Thereby, we investigate if the weight-bearingline alignment method results in short term (within 2 weeks) physical complaints

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)