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NCT06225245 · ClinicalTrials.gov registry record · NA

Augmenting Rehabilitation Outcomes and Functional Neuroplasticity Using Epidural Stimulation of Cervical Spinal Cord

A NA study of Spinal Cord Injuries and Cervical Spinal Cord Injury, sponsored by The Methodist Hospital Research Institute.

Recruiting
Registry status
NA
Development phase
12
Enrollment target
1
Study location

NCT06225245 is a NA study of Spinal Cord Injuries and Cervical Spinal Cord Injury that is actively recruiting participants, run by The Methodist Hospital Research Institute. The registered enrollment target is 12 participants, below the 62-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06225245, a NA study of Spinal Cord Injuries and Cervical Spinal Cord Injury, is actively recruiting participants, sponsored by The Methodist Hospital Research Institute.

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

Study Summary

The goal of this study is to investigate the effects of cervical epidural spinal stimulation with upper extremity training. This is an investigational study. The device used for epidural spinal stimulation (ESS) to deliver spinal stimulation is called the CoverEdgeX 32 Surgical Lead system. This device is approved by the Food and Drug Administration (FDA) for the treatment of severe pain and to manage chronic pain when other treatments have not been effective. In this study, the device is considered an investigational device because it is not approved for use in the treatment of spinal cord injury

Interventions

  • DEVICE Epidural Spinal Stimulation (ESS)

Study Locations (1)

Texas

  • The Methodist Hospital Research Institute - Houston

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2024-08-06
Est. Completion 2027-01-01
Phase NA

What the Registry Record Tells You About NCT06225245

The ClinicalTrials.gov registry entry for NCT06225245 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 62-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (81% lower). The listed sponsor is The Methodist Hospital Research Institute, which has 126 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Spinal Cord Injuries appearing as the primary indexed condition, and to 1 intervention - of which Epidural Spinal Stimulation (ESS) is the first listed.

NCT06225245 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06225245 about?

NCT06225245 is a clinical study titled "Augmenting Rehabilitation Outcomes and Functional Neuroplasticity Using Epidural Stimulation of Cervical Spinal Cord". The goal of this study is to investigate the effects of cervical epidural spinal stimulation with upper extremity training. This is an investigational study. The device used for epidural spinal stimulation (ESS) to deliver spinal stimulation is called the CoverEdgeX 32 Surgical Lead system. This de...

What is the current status of trial NCT06225245?

This trial is currently recruiting. It is a NA study. The enrollment target is 12 participants. The study started on 2024-08-06. Estimated completion is 2027-01-01.

What conditions does trial NCT06225245 study?

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

What interventions are being tested in trial NCT06225245?

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

Who is sponsoring clinical trial NCT06225245?

This trial is sponsored by The Methodist Hospital Research Institute, which has 126 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06225245 being conducted?

This trial has 1 study location across Texas. 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

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