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NCT03260400 · ClinicalTrials.gov registry record · NA
Short-term Implanted Electrodes Following Regenerative Peripheral Nerve Surgery for Improving Prosthetic Limb Control Signals
A NA study of Amputation and Amputation Neuroma, sponsored by University of Michigan.
- Recruiting
- Registry status
- NA
- Development phase
- 10
- Enrollment target
- 1
- Study location
NCT03260400 is a NA study of Amputation and Amputation Neuroma that is actively recruiting participants, run by University of Michigan. The registered enrollment target is 10 participants, below the 133-participant average among 65 other Amputation trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03260400, a NA study of Amputation and Amputation Neuroma, is actively recruiting participants, sponsored by University of Michigan.
- RECRUITING
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
- 1
- Study location
Study Summary
The device, a bipolar percutaneous intramuscular electromyography electrode, is intended for use in upper-limb amputation patients who have received the regenerative peripheral nerve interface surgical procedure, in order to enable the use of advanced prosthetic arms and hands.
Conditions Studied
Interventions
- DEVICE a bipolar percutaneous intramuscular electromyography electrode
Study Locations (1)
Michigan
- University of Michigan - Ann Arbor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2017-12-11 |
| Est. Completion | 2029-05-05 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03260400
The ClinicalTrials.gov registry entry for NCT03260400 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 133-participant average among 65 other Amputation trials with a reported enrollment target (92% lower). The listed sponsor is University of Michigan, which has 1,327 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Amputation appearing as the primary indexed condition, and to 1 intervention - of which a bipolar percutaneous intramuscular electromyography electrode is the first listed.
NCT03260400 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.
Frequently Asked Questions
What is clinical trial NCT03260400 about?
NCT03260400 is a clinical study titled "Short-term Implanted Electrodes Following Regenerative Peripheral Nerve Surgery for Improving Prosthetic Limb Control Signals". The device, a bipolar percutaneous intramuscular electromyography electrode, is intended for use in upper-limb amputation patients who have received the regenerative peripheral nerve interface surgical procedure, in order to enable the use of advanced prosthetic arms and hands.
What is the current status of trial NCT03260400?
This trial is currently recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2017-12-11. Estimated completion is 2029-05-05.
What conditions does trial NCT03260400 study?
This clinical trial studies the following conditions: Amputation, Amputation Neuroma.
What interventions are being tested in trial NCT03260400?
The interventions under investigation include: a bipolar percutaneous intramuscular electromyography electrode (DEVICE).
Who is sponsoring clinical trial NCT03260400?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03260400 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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