Clinical Trials in the USA / NCT07915700
Recruiting
Not applicable
Hand Prosthesis Usability and Performance
NCT07915700 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Amputation
Investigational drug(s) / intervention(s)
Prototype hand prosthesisBaseline Comparator Device
Prototype hand prosthesis: Prototype hand prosthesis
Baseline Comparator Device: All participants will use their own prosthesis
Study summary
This study asks individuals with upper limb absence to use a new hand prosthesis, and compare it's performance to their own hand prosthesis
Eligibility
Inclusion Criteria:
* Multi-articulating hand experience
* At least 18 years old
* Transradial, acquired amputation or congenital upper limb absence
* Unilateral upper limb absence preferred Good socket comfort in own prosthesis (\>/= 6 on Hanspal socket comfort score)
Exclusion Criteria:
* Any health conditions that pose a risk to participation in study events (in the opinion of the Investigator), e.g. Visual impairment; Cognitive impairment
* Cognitively unable to provide informed consent or comply with the study procedures
Primary outcome measure(s)
- Grip Accuracy — At baseline and each post-treatment visit (x3 visits over 12 weeks)
Functional observer rated test of ability to perform grips. This test assesses the feasibility that the device can be used as a reliable hand prosthesis when operated by the intended use population. An observer rates the successful achievement of the prompted outcome on a 0-3 scale (0= no output, 3= output achieved without error). The four grips (hand open, hand close, thumb rotation to palm, thumb rotation away from palm) are repeated x3, resulting in a minimum summary score of 0 or a maximum summary score of 36.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Ossur Americas | Dublin | Ohio | Recruiting |
More Össur Iceland ehf trials in the USA
Pro APP Prosthetic Outcome Registry
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Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07915700 on ClinicalTrials.gov ↗ ← All trials in the USA