Clinical Feasibility of the IMES Transradial Prosthesis
ConditionAmputation
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorÖssur Iceland ehf
About this trial
This study will evaluate the feasibility of using implanted myoelectric sensors (IMES) to control a transradial prosthesis
Eligibility criteria
Qualifiers
(unilateral acquired transradial) amputation
residual limb size requirements to fit investigational device componentry
at least 6 residual muscle locations available for implantation
good compliance with health service (rehabilitation)
Disqualifiers
any condition which in the opinion of the investigator poses a risk to health
neurological disorder that may prohibit accurate control
major injury proximal to the level of amputation
neuromuscular disorder
Trial design
Treatments tested in this trial
- IMES
Treatment groups
3 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov