Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06701422 · ClinicalTrials.gov registry record · NA
Targeting Cervical Epidural Spinal Cord Stimulation for Functional Recovery
A NA study of Cervical Spinal Cord Injury and Tetraplegia/Tetraparesis, sponsored by Columbia University.
- Recruiting
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 2
- Study locations
NCT06701422 is a NA study of Cervical Spinal Cord Injury and Tetraplegia/Tetraparesis that is actively recruiting participants, run by Columbia University. The registered enrollment target is 36 participants, above the 20-participant average among 18 other Cervical Spinal Cord Injury trials with a reported enrollment target (80% higher). The trial reports 2 study locations across 1 state.
The verdict
NCT06701422, a NA study of Cervical Spinal Cord Injury and Tetraplegia/Tetraparesis, is actively recruiting participants, sponsored by Columbia University.
- RECRUITING
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 2
- Study locations
Study Summary
The proposed study seeks to understand how the cervical spinal cord should be stimulated after injury through short-term physiology experiments that will inform a preclinical efficacy trial. The purpose of this study is to determine which cervical levels epidural electrical stimulation (EES) should target to recruit arm and hand muscles effectively and selectively in spinal cord injury (SCI).
Conditions Studied
Interventions
- PROCEDURE Intraoperative stimulation of the cervical spinal cord
Study Locations (2)
New York
- Columbia University Irving Medical Center - New York
- The Daniel and Jane Och Spine Hospital at NewYork-Presbyterian/Allen - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2024-12-06 |
| Est. Completion | 2026-06-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06701422
The ClinicalTrials.gov registry entry for NCT06701422 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 20-participant average among 18 other Cervical Spinal Cord Injury trials with a reported enrollment target (80% higher). The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Cervical Spinal Cord Injury appearing as the primary indexed condition, and to 1 intervention - of which Intraoperative stimulation of the cervical spinal cord is the first listed.
NCT06701422 reports 2 study locations spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT06701422 about?
NCT06701422 is a clinical study titled "Targeting Cervical Epidural Spinal Cord Stimulation for Functional Recovery". The proposed study seeks to understand how the cervical spinal cord should be stimulated after injury through short-term physiology experiments that will inform a preclinical efficacy trial. The purpose of this study is to determine which cervical levels epidural electrical stimulation (EES) should ...
What is the current status of trial NCT06701422?
This trial is currently recruiting. It is a NA study. The enrollment target is 36 participants. The study started on 2024-12-06. Estimated completion is 2026-06-30.
What conditions does trial NCT06701422 study?
This clinical trial studies the following conditions: Cervical Spinal Cord Injury, Tetraplegia/Tetraparesis, Cervical Myelopathy.
What interventions are being tested in trial NCT06701422?
The interventions under investigation include: Intraoperative stimulation of the cervical spinal cord (PROCEDURE).
Who is sponsoring clinical trial NCT06701422?
This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06701422 being conducted?
This trial has 2 study locations across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Cervical Spinal Cord Injury
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Precise Robotically IMplanted Brain-Computer InterfacE
RECRUITING · NA
-
Neurostimulation for Respiratory Function After Spinal Cord Injury
RECRUITING · NA
-
Connect-One: Early Feasibility Study of Connexus® Brain-Computer Interface (BCI)
RECRUITING · NA
-
Feasibility of the BrainGate2 Neural Interface System in Persons With Tetraplegia (BG-Tablet-01)
RECRUITING · NA
-
Augmenting Rehabilitation Outcomes and Functional Neuroplasticity Using Epidural Stimulation of Cervical Spinal Cord
RECRUITING · NA
-
A User-friendly, Non-invasive Neuro-orthosis That Restores Volitionally Controlled Grasp Functions for SCI Survivors With Tetraplegia
RECRUITING · NA
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
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.