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NCT06410001 · ClinicalTrials.gov registry record · Phase 1

CE-STAND: Cervical Epidural STimulation After Neurologic Damage

A Phase 1 study of Spinal Cord Injury, sponsored by University of Minnesota.

Recruiting
Registry status
Phase 1
Development phase
36
Enrollment target
1
Study location

NCT06410001 is a Phase 1 study of Spinal Cord Injury that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 36 participants, below the 86-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (58% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06410001, a Phase 1 study of Spinal Cord Injury, is actively recruiting participants, sponsored by University of Minnesota.

RECRUITING
Registry status
Phase 1
Development phase
36 participants
Enrollment target
1
Study location

Study Summary

CE-STAND aims to address three areas under-represented in research: chronic, cervical, and autonomic dysfunction. It is both significant and highly impactful, as treating autonomic dysfunction could substantially improve function and quality of life (QoL) in chronic cervical SCI patients.

Conditions Studied

Spinal Cord Injury

Interventions

  • DEVICE Epidural Spinal Cord Stimulation System

Study Locations (1)

Minnesota

  • University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2026-03-01
Est. Completion 2030-07-30
Phase Phase 1

Sponsor

University of Minnesota

966 total trials

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What the Registry Record Tells You About NCT06410001

The ClinicalTrials.gov registry entry for NCT06410001 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 86-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (58% lower). The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Spinal Cord Injury appearing as the primary indexed condition, and to 1 intervention - of which Epidural Spinal Cord Stimulation System is the first listed.

NCT06410001 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT06410001 about?

NCT06410001 is a clinical study titled "CE-STAND: Cervical Epidural STimulation After Neurologic Damage". CE-STAND aims to address three areas under-represented in research: chronic, cervical, and autonomic dysfunction. It is both significant and highly impactful, as treating autonomic dysfunction could substantially improve function and quality of life (QoL) in chronic cervical SCI patients.

What is the current status of trial NCT06410001?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2026-03-01. Estimated completion is 2030-07-30.

What conditions does trial NCT06410001 study?

This clinical trial studies the following conditions: Spinal Cord Injury.

What interventions are being tested in trial NCT06410001?

The interventions under investigation include: Epidural Spinal Cord Stimulation System (DEVICE).

Who is sponsoring clinical trial NCT06410001?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06410001 being conducted?

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

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.