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NCT07075198 · ClinicalTrials.gov registry record · NA
Caesar Foot Take-Home Validation Testing
A NA study of Prosthesis User and Lower Limb Amputation Below Knee (Injury), sponsored by Liberating Technologies.
- Recruiting
- Registry status
- NA
- Development phase
- 18
- Enrollment target
- 1
- Study location
NCT07075198 is a NA study of Prosthesis User and Lower Limb Amputation Below Knee (Injury) that is actively recruiting participants, run by Liberating Technologies. The registered enrollment target is 18 participants, below the 56-participant average among 12 other Prosthesis User trials with a reported enrollment target (68% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07075198, a NA study of Prosthesis User and Lower Limb Amputation Below Knee (Injury), is actively recruiting participants, sponsored by Liberating Technologies.
- RECRUITING
- Registry status
- NA
- Development phase
- 18 participants
- Enrollment target
- 1
- Study location
Study Summary
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 surveys and performance-based measures will be collected in the clinic at the end of each condition. The intent of this study is to determine the Caesar foot's feasibility in a real-world environment. Data will be collected to understand impact to the user's daily life and physical activity through outcomes and participant feedback. The feedback obtained during this study will be essential to informing the design intended for commercialization.
Conditions Studied
Interventions
- DEVICE Caesar Foot
Study Locations (1)
Texas
- Hanger Clinic - Austin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2025-10 |
| Est. Completion | 2026-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07075198
The ClinicalTrials.gov registry entry for NCT07075198 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 56-participant average among 12 other Prosthesis User trials with a reported enrollment target (68% lower). The listed sponsor is Liberating Technologies, which has 13 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Prosthesis User appearing as the primary indexed condition, and to 1 intervention - of which Caesar Foot is the first listed.
NCT07075198 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT07075198 about?
NCT07075198 is a clinical study titled "Caesar Foot Take-Home Validation Testing". 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...
What is the current status of trial NCT07075198?
This trial is currently recruiting. It is a NA study. The enrollment target is 18 participants. The study started on 2025-10. Estimated completion is 2026-08.
What conditions does trial NCT07075198 study?
This clinical trial studies the following conditions: Prosthesis User, Lower Limb Amputation Below Knee (Injury).
What interventions are being tested in trial NCT07075198?
The interventions under investigation include: Caesar Foot (DEVICE).
Who is sponsoring clinical trial NCT07075198?
This trial is sponsored by Liberating Technologies, which has 13 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07075198 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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