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.
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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

Jennifer Johansson

774-233-0874

jen.johansson@liberatingtech.com

CONTACT

Brianna Rozell

774-233-0876

brianna.rozell@liberatingtech.com

CONTACT