To Evaluate the Clinical Impact of the Point Powered System
Starting soon · Not applicable
Conditions studied: Amputation; Traumatic, Hand
In brief
The objective of this study is to evaluate the efficacy of the Point Powered system as compared to the patient's standard-of-care treatment. This study will be a single subject crossover design where one group of 10 adult partial hand amputees will be evaluated on several metrics on their existing prosthetic treatment (Treatment 1) and the Point Powered system (Treatment 2) over a period of three months using standard two-site myoelectric control. Metrics include: in-clinic functional measures, subjective assessments, bilateral hand use, and prosthesis wear time.
Key facts
- Study ID
- NCT07135947
- Run by
- Point Designs
- People needed
- 10
- Starts
- 2026-09-01
- Expected to finish
- 2027-04-01
- Last updated by the study team
- 2026-06-26
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Partial unilateral hand loss with at least index and/or middle fingers amputated at the MCP level
- Intact thumb with full range of motion
- Fluent in English
- Age of 18 years or older
You may not qualify if…
- Patients with a residual limb that is unhealed from the amputation surgery
- Unhealed wounds
- Significant cognitive deficits as determined upon clinical evaluation
- Significant neurological deficits as determined upon clinical evaluation
- Significant physical deficits of the residual limb impacting full participation in the study as determined upon clinical evaluation
- Uncontrolled pain or phantom pain impacting full participation in the study as determined upon clinical evaluation
- Serious uncontrolled medical problems as judged by the project therapist
Where it is running
- University of Colorado Denver | Anschutz Medical Campus — Aurora, Colorado, United States
- Point Designs — Broomfield, Colorado, United States
- Hanger Clinic — Lafayette, Colorado, United States
Full record on ClinicalTrials.gov
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