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NCT03409133 · ClinicalTrials.gov registry record · NA

Feasibility of Neural Feedback for Lower Limb Amputees

A NA study of Amputation, sponsored by Louis Stokes VA Medical Center.

Recruiting
Registry status
NA
Development phase
15
Enrollment target
1
Study location

NCT03409133 is a NA study of Amputation that is actively recruiting participants, run by Louis Stokes VA Medical Center. The registered enrollment target is 15 participants, below the 133-participant average among 65 other Amputation trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03409133, a NA study of Amputation, is actively recruiting participants, sponsored by Louis Stokes VA Medical Center.

RECRUITING
Registry status
NA
Development phase
15 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the effectiveness of providing sensation of the missing limb to individuals with lower limb loss, including above and below knee amputees. The approach involves delivering small electrical currents directly to remaining nerves via implanted stimulating electrodes. These small electrical currents cause the nerves to generate signals that are then transferred to your brain similar to how information about the foot and lower limb used to be transferred to your brain prior to the amputation. Individuals also have the option to have recording electrodes implanted within muscles of the lower limb(s) in an attempt to develop a motor controller that would enable the user to have intuitive control of a robotic prosthetic leg.

Conditions Studied

Interventions

  • DEVICE Stimulating nerve electrodes and intramuscular recording electrodes

Study Locations (1)

Ohio

  • Louis Stokes VA Medical Center - Cleveland

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2015-11-05
Est. Completion 2027-09-01
Phase NA

Sponsor

Louis Stokes VA Medical Center

10 total trials

What the Registry Record Tells You About NCT03409133

The ClinicalTrials.gov registry entry for NCT03409133 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 15 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 (89% lower). The listed sponsor is Louis Stokes VA Medical Center, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Amputation appearing as the primary indexed condition, and to 1 intervention - of which Stimulating nerve electrodes and intramuscular recording electrodes is the first listed.

NCT03409133 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT03409133 about?

NCT03409133 is a clinical study titled "Feasibility of Neural Feedback for Lower Limb Amputees". The purpose of this study is to evaluate the effectiveness of providing sensation of the missing limb to individuals with lower limb loss, including above and below knee amputees. The approach involves delivering small electrical currents directly to remaining nerves via implanted stimulating electr...

What is the current status of trial NCT03409133?

This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2015-11-05. Estimated completion is 2027-09-01.

What conditions does trial NCT03409133 study?

This clinical trial studies the following conditions: Amputation.

What interventions are being tested in trial NCT03409133?

The interventions under investigation include: Stimulating nerve electrodes and intramuscular recording electrodes (DEVICE).

Who is sponsoring clinical trial NCT03409133?

This trial is sponsored by Louis Stokes VA Medical Center, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03409133 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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