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Clinical Trials/NL-OMON49303
NL-OMON49303
Completed
N/A

Evaluation of a new powered knee prosthesis (Reboocon IntelLeg Knee) - Evaluation of Reboocon IntelLeg Knee

Reboocon Bionics (medeverrichter naast de Universiteit Twente)0 sites16 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Reboocon Bionics (medeverrichter naast de Universiteit Twente)
Enrollment
16
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Reboocon Bionics (medeverrichter naast de Universiteit Twente)

Eligibility Criteria

Inclusion Criteria

  • Individuals without an amputation
  • \- Aged between 18 and 65\.
  • \- Body length between 1\.20 and 1\.95 m.
  • \- Weight below 125 kg.
  • \- Able to perform low to moderate vigorous physical activity for a duration of
  • 3 hours including breaks., Individuals with an amputation
  • \- Aged between 18 and 65\.
  • \- Weight below 125 kg.
  • \- Body length between 1\.20 and 1\.95 m.
  • \- Unilateral transfemoral amputation or knee disarticulation.

Exclusion Criteria

  • Individuals without an amputation:
  • \- Not willing to consent to participate in the study.
  • \- Musculoskeletal problems influencing walking ability., Individuals with an
  • amputation:
  • \- Not willing to consent to participate in the study.
  • \- Other musculoskeletal problems influencing walking ability.
  • \- Stump problems/bad socket fitting, Only for study I (for both individuals
  • with and individuals without amputation):
  • \- For the second and third individual with amputation, subject\*s weight differs
  • more than 15 kg of already included subject(s) or subject\*s length differs

Outcomes

Primary Outcomes

Not specified

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