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RECRUITING Not applicable ClinicalTrials.gov

Cross-Over Study Evaluating the TASKA GEN2 Myoelectric Hand Prosthesis

Sponsor: TASKA Prosthetics • ClinicalTrials.gov ID: NCT07876115

Registry updated: 2026-10-15
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Description

This prospective multicentre randomized cross-over post-market clinical follow-up study compares the TASKA GEN2 multi-grip myoelectric hand prosthesis with marketed comparator prostheses in adults with upper-limb amputation. The study evaluates specific function using the Patient-Specific Functional Scale together with upper-limb function, comfort, quality of life, satisfaction and safety outcomes.

Interventions

  • TASKA GEN2 Multi-Grip Myoelectric Hand Prosthesis (Device)
    Participants use the Taska Gen2 multi-grip myoelectric prosthesis
  • Michelangelo or I-Limb Ultra multi-grip myoelectric prosthesis (Device)
    Participants use their usual marketed multi-grip myoelectric hand prosthesis (Michelangelo or I-Limb Ultra) during the relevant 28-day study period.

Eligibility criteria

Inclusion Criteria: * Adult patient (\>18 years). * Unilateral acquired or congenital transradial or transhumeral amputation or elbow disarticulation. * Using Michelangelo or I-Limb Ultra prosthesis for \>2 months. * Prosthesis use \>6 hours/day. * Written informed consent. Exclusion Criteria: * Bilateral upper-limb amputation. * Shoulder disarticulation. * Lower-limb amputation. * Temporary prosthesis. * Major expected routine activity change. * Progressive pathology preventing follow-up. * Pregnancy. * Protected/vulnerable adults. * No health insurance affiliation. * Unable to understand study instructions.

Conditions

Upper Limb Amputation Transradial Amputation Transhumeral Amputation

Locations

  • Multiple facilities — Multiple Locations, France
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record