Epidermal Sensors for Wireless and Enhanced Amputee Skin Tracking (E-SWEAT) Part 1

Recruiting Phase 1 Interventional Study
Transtibial Amputation
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Device Feasibility
Participants needed
16 (estimated)
Sponsor
North Carolina State University · Other
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About This Trial
The goal of this clinical trial is to 1) demonstrate the feasibility of monitoring pressure, temperature, and lactic acid density of sweat inside the prosthetic socket, and 2) verify the relationship between mechanical pressure and Lactic acid density of sweat for lower limb amputees among transtibial amputees. The main questions it aims to answer are: * Is it feasible to reliably monitor pressur…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Be 18 years or older * Have a unilateral lower limb amputee (below the knee). The tibial length on the residual limb must be greater than half of the length of the tibial on the unaffected side * Have an amputation that occurred over 2 years ago * Have at least 1 year of exper…
Contacts

Amay Bandodkar, PhD

9195150417

ajbandod@ncsu.edu

CONTACT

Ming Liu, PhD

9195158541

mliu10@ncsu.edu

CONTACT