Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Neural Enabled Prosthesis for Upper Limb Amputees

NCT03432325 · View on ClinicalTrials.gov ↗

Study Summary

This study is designed to evaluate the feasibility of The Adaptive Neural Systems Neural-Enabled Prosthetic Hand (ANS-NEPH) system.

Interventions

  • DEVICE Neural Enabled Prosthesis

Study Locations (2)

Arkansas

  • University of Arkansas — Fayetteville

Maryland

  • Walter Reed National Military Medical Center — Bethesda

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2017-12-14
Est. Completion 2025-12-31
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03432325

The ClinicalTrials.gov registry entry for NCT03432325 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Arkansas, Fayetteville, which has 40 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Prosthesis User appearing as the primary indexed condition, and to 1 intervention — of which Neural Enabled Prosthesis is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03432325 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Arkansas, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03432325 about?

NCT03432325 is a clinical study titled "Neural Enabled Prosthesis for Upper Limb Amputees". This study is designed to evaluate the feasibility of The Adaptive Neural Systems Neural-Enabled Prosthetic Hand (ANS-NEPH) system.

What is the current status of trial NCT03432325?

This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2017-12-14. Estimated completion is 2025-12-31.

What conditions does trial NCT03432325 study?

This clinical trial studies the following conditions: Prosthesis User, Amputation Arm and Hand, Unilateral Right, Amputation Arm and Hand, Unilateral Left. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03432325?

The interventions under investigation include: Neural Enabled Prosthesis (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03432325?

This trial is sponsored by University of Arkansas, Fayetteville, which has 40 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03432325 being conducted?

This trial has 2 study locations across Arkansas, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial