Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01546675 · ClinicalTrials.gov registry record · NA
Interface Kinematics of Transhumeral Prosthetic Sockets Using XROMM
A NA study of Traumatic Amputation of Arm, sponsored by US Department of Veterans Affairs.
- Completed
- Registry status
- NA
- Development phase
- 2
- Enrollment target
- 2
- Study locations
NCT01546675: Completed NA study of Traumatic Amputation of Arm, sponsored by US Department of Veterans Affairs.
NCT01546675 is a NA study of Traumatic Amputation of Arm that has completed, run by US Department of Veterans Affairs. The registered enrollment target is 2 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01546675, a NA study of Traumatic Amputation of Arm, has completed, sponsored by US Department of Veterans Affairs.
- COMPLETED
- Registry status
- NA
- Development phase
- 2 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this pilot study was to conduct a head-to-head comparison of two designs for transhumeral level upper limb prosthetic sockets: a traditional socket design and a socket design hypothesized to provide greater skeletal stabilization. The investigators comparisons included assessments of patient comfort and satisfaction with fit, as well as dynamic kinematic assessment using X-Ray Reconstruction of Moving Morphology (XROMM) a novel high-speed, high-resolution, bi-plane video radiography system.
Primary Outcome
Shoulder abduction was performed to the subject's maximum elevation. Skeletal and socket kinematics were calculated using the markerless auto-registration algorithm and X-Ray Reconstruction of Moving Morphology (XROMM)
Conditions Studied
Interventions
- OTHER Skeletal Stabilization
Study Locations (2)
New York
- Manhattan Campus of the VA NY Harbor Healthcare System, New York, NY - New York
Rhode Island
- Providence VA Medical Center, Providence, RI - Providence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2 participants |
| Start Date | 2012-01 |
| Est. Completion | 2013-09 |
| Phase | NA |
What the finished NCT01546675 record still lists
NCT01546675 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 1 condition, with Traumatic Amputation of Arm appearing as the primary indexed condition, and to 1 intervention - of which Skeletal Stabilization is the first listed.
NCT01546675 reports a single indexed study location in New York, Rhode Island.
Frequently Asked Questions
What is clinical trial NCT01546675 about?
NCT01546675 is a clinical study titled "Interface Kinematics of Transhumeral Prosthetic Sockets Using XROMM". The purpose of this pilot study was to conduct a head-to-head comparison of two designs for transhumeral level upper limb prosthetic sockets: a traditional socket design and a socket design hypothesized to provide greater skeletal stabilization. The investigators comparisons included assessments of ...
What is the current status of trial NCT01546675?
This trial is currently completed. It is a NA study. The enrollment target is 2 participants. The study started on 2012-01. Estimated completion is 2013-09.
What conditions does trial NCT01546675 study?
This clinical trial studies the following conditions: Traumatic Amputation of Arm.
What interventions are being tested in trial NCT01546675?
The interventions under investigation include: Skeletal Stabilization (OTHER).
Who is sponsoring clinical trial NCT01546675?
This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01546675 being conducted?
This trial has 2 study locations across New York, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01546675's enrollment target sits among peer trials
2 1997th of 2000 the lowest 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
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia