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NCT05012683 · ClinicalTrials.gov registry record · NA
To Assess the Utility of the Point Partial in a Clinical Take-home Study of Partial Hand Amputees
A NA study, sponsored by Point Designs.
- Completed
- Registry status
- NA
- Development phase
- 11
- Enrollment target
NCT05012683: Completed NA study, sponsored by Point Designs.
NCT05012683 is a NA study that has completed, run by Point Designs. The registered enrollment target is 11 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05012683, a NA study, has completed, sponsored by Point Designs.
- COMPLETED
- Registry status
- NA
- Development phase
- 11 participants
- Enrollment target
Study Summary
This study will allow us to assess whether the Point Partial confers functional and psychological benefit to persons with partial finger amputations in an unconstrained environment. The use of the Point Partial outside of the laboratory will allow for a wider variety of uses and for a more realistic simulation of the product being used in the field. This well-controlled trial (without randomization of subjects) will produce the first Level II-1 medical evidence in our field of partial hand prosthetic design as described by the 1989 U.S. Preventive Services Task Force. Furthermore, this study will provide important data to support providers who are requesting reimbursement from payers.
Primary Outcome
Capacity Assessment of Prosthetic Performance for the Upper Limb (CAPPFUL) provides a comprehensive, performance based measure for upper limb prosthetic use with any upper-limb functional prosthesis at any amputation level through assessment of commonplace activities that take place in various planes of movement. Scale Title: Overall Performance. Scale Minimum: 0. Scale Maximum: 100. Higher score indicates better outcome.
Interventions
- DEVICE Point Partial
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2021-01-05 |
| Est. Completion | 2022-12-31 |
| Phase | NA |
What the finished NCT05012683 record still lists
NCT05012683 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Point Partial is the first listed.
NCT05012683 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05012683 about?
NCT05012683 is a clinical study titled "To Assess the Utility of the Point Partial in a Clinical Take-home Study of Partial Hand Amputees". This study will allow us to assess whether the Point Partial confers functional and psychological benefit to persons with partial finger amputations in an unconstrained environment. The use of the Point Partial outside of the laboratory will allow for a wider variety of uses and for a more realistic...
What is the current status of trial NCT05012683?
This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2021-01-05. Estimated completion is 2022-12-31.
What interventions are being tested in trial NCT05012683?
The interventions under investigation include: Point Partial (DEVICE).
Who is sponsoring clinical trial NCT05012683?
This trial is sponsored by Point Designs, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05012683's enrollment target sits among peer trials
11 1927th of 2000 higher than 74 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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