IMES Prosthesis for Transradial Amputation

Clinical Feasibility of the IMES Transradial Prosthesis

Recruiting N/A Interventional Study
Amputation
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 65
Sex
Any
Study type
Interventional
Purpose
Device Feasibility
Participants needed
3 (estimated)
Sponsor
Össur Iceland ehf · Industry
Who this trial is looking for

This trial is looking for people who have lost their arm below the elbow and want to try a new type of prosthetic device. Participants will have a device implanted that uses sensors to help control the prosthetic arm.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have a below-elbow arm amputation.
  • I am willing to have sensors implanted in my arm.
  • I have at least 6 muscle areas available for the sensors.
  • I have experience using myoelectric prostheses.
  • I use my myoelectric device for about 6-8 hours each day.
  • I can attend study visits and give consent.

You may not be able to join if

  • I have a health condition that may pose a risk.
  • I have a neurological disorder affecting control.
  • I have a major injury above the amputation level.
  • I have a neuromuscular disorder.
  • I have nerve damage that could affect the muscles for implantation.
  • I am allergic to materials used in implants.
  • I already have an active implant.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

This study will evaluate the feasibility of using implanted myoelectric sensors (IMES) to control a transradial prosthesis

Trial Locations

Sorted by distance from Iowa

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Eligibility Criteria
Inclusion Criteria: * (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) * willing to undergo surgical impla…
Contacts

Daire McGuinness, BSc

00441315070097

dmcguinness@ossur.com

CONTACT