Point Partial for Hand Amputation

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Hand AmputationPoint Partial - Device
Eligibility
18+
All Sexes
What conditions do you have?
Select

Study Summary

This trial will test how well the Point Partial works for people with partial finger amputations in everyday settings, and will provide evidence to support reimbursement from payers.

Eligible Conditions
  • Hand Amputation

Treatment Effectiveness

Study Objectives

4 Primary · 0 Secondary · Reporting Duration: ~Day 60: with prosthesis, 60 days post-fitting

Day 60
Upper Extremity
Disability of the Arm, Shoulder and Hand (DASH)
EuroQol-5 Dimension (EQ-5D-5L)
Southampton Hand Assessment Procedure (SHAP)

Trial Safety

Trial Design

2 Treatment Groups

No Prosthesis
1 of 2
Prosthesis
1 of 2

Active Control

Experimental Treatment

11 Total Participants · 2 Treatment Groups

Primary Treatment: Point Partial · No Placebo Group · N/A

Prosthesis
Device
Experimental Group · 1 Intervention: Point Partial · Intervention Types: Device
No ProsthesisNoIntervention Group · 1 Intervention: No Prosthesis · Intervention Types:

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: ~day 60: with prosthesis, 60 days post-fitting

Who is running the clinical trial?

Arm DynamicsUNKNOWN
1 Previous Clinical Trials
11 Total Patients Enrolled
Point DesignsLead Sponsor
4 Previous Clinical Trials
33 Total Patients Enrolled
University of Colorado, DenverOTHER
1,594 Previous Clinical Trials
1,927,385 Total Patients Enrolled

Eligibility Criteria

Age 18+ · All Participants · 4 Total Inclusion Criteria

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