Caesar Foot Take-Home Validation Testing
Recruiting
N/A
Interventional Study
Prosthesis User
Lower Limb Amputation Below Knee (Injury)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 18 (estimated)
- Sponsor
- Liberating Technologies, Inc. · Industry
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About This Trial
The rationale for this study is to conduct a take-home clinical trial to evaluate the impact of the bimodal Caesar foot in a real-world environment. Participants will take the device home and use it throughout their daily life for two months. A one-month baseline period, using their usual foot, will be completed both before and after the two-month period with the Caesar foot condition. Self-report…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Have transtibial limb absence of one or both limbs
* Express interest in running, but do not currently have a running blade (as determined by self-report)
* Are at least 18 years of age
* Are at least six months post amputation
* Are classified as K3 or K4 ambulator status as …
Contacts