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NCT07225582 · ClinicalTrials.gov registry record · NA
Development of Optimal Sensory Feedback Strategies to Maximize Function After Tetraplegia
A NA study of Spinal Cord Injury Cervical and Spinal Cord Injuries (Complete and Incomplete), sponsored by Case Western Reserve University.
- Recruiting
- Registry status
- NA
- Development phase
- 3
- Enrollment target
- 1
- Study location
NCT07225582: Recruiting NA study of Spinal Cord Injury Cervical and Spinal Cord Injuries (Complete and Incomplete), sponsored by Case Western Reserve University.
NCT07225582 is a NA study of Spinal Cord Injury Cervical and Spinal Cord Injuries (Complete and Incomplete) that is actively recruiting participants, run by Case Western Reserve University. The registered enrollment target is 3 participants, below the 20-participant average among 12 other Spinal Cord Injury Cervical trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07225582, a NA study of Spinal Cord Injury Cervical and Spinal Cord Injuries (Complete and Incomplete), is actively recruiting participants, sponsored by Case Western Reserve University.
- RECRUITING
- Registry status
- NA
- Development phase
- 3 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to learn more about how stimulating the nerves involved in sensation (either in the limbs or in the brain) can be used to restore sensation in participants who have a spinal cord injury. Participants in this study will have already been enrolled in the "Reconnecting the Hand and Arm to the Brain (ReHAB)" study, and received small electrodes in a part of the brain that is involved in sensing touch and pressure in the hand. The ReHAB study participants will also have received electrodes around the nerves in their arm. In this clinical trial, participants will receive two types of electrical stimulation: * Intracortical microstimulation (ICMS) which involves sending small electrical pulses to the part of the brain that processes sensation. * Peripheral nerve stimulation (PNS) which involves sending small electrical pulses to the nerves in the arm that transmit sensations from the hand. Researchers will try different patterns of stimulation for both ICMS and PNS and study how the participants perceive the sensations from the different stimulation patterns. The researchers will also study how combining ICMS and PNS affects the perceived sensations.
Primary Outcome
Percentage of force matching trials per block in which the target force was achieved before the time limit
Conditions Studied
Interventions
- DEVICE Brain Computer Interface (BCI) - Functional Electrical Stimulation (FES) system
Study Locations (1)
Ohio
- Case Western Reserve University - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 3 participants |
| Start Date | 2026-01-13 |
| Est. Completion | 2030-09-01 |
| Phase | NA |
What NCT07225582 shows while recruiting
NCT07225582 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 20-participant average among 12 other Spinal Cord Injury Cervical trials with a reported enrollment target (85% lower).
The record links to 2 conditions, with Spinal Cord Injury Cervical appearing as the primary indexed condition, and to 1 intervention - of which Brain Computer Interface (BCI) - Functional Electrical Stimulation (FES) system is the first listed.
NCT07225582 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT07225582 about?
NCT07225582 is a clinical study titled "Development of Optimal Sensory Feedback Strategies to Maximize Function After Tetraplegia". The goal of this clinical trial is to learn more about how stimulating the nerves involved in sensation (either in the limbs or in the brain) can be used to restore sensation in participants who have a spinal cord injury. Participants in this study will have already been enrolled in the "Reconnectin...
What is the current status of trial NCT07225582?
This trial is currently recruiting. It is a NA study. The enrollment target is 3 participants. The study started on 2026-01-13. Estimated completion is 2030-09-01.
What conditions does trial NCT07225582 study?
This clinical trial studies the following conditions: Spinal Cord Injury Cervical, Spinal Cord Injuries (Complete and Incomplete).
What interventions are being tested in trial NCT07225582?
The interventions under investigation include: Brain Computer Interface (BCI) - Functional Electrical Stimulation (FES) system (DEVICE).
Who is sponsoring clinical trial NCT07225582?
This trial is sponsored by Case Western Reserve University, which has 141 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07225582 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Spinal Cord Injury Cervical
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.
Where NCT07225582's enrollment target sits among peer trials
3 13th of 12 the lowest of 12 other Spinal Cord Injury Cervical trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Spinal Cord Injury Cervical trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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Combining Spinal Cord Transcutaneous Stimulation and Activity-based Training in Inpatient Rehabilitation to Facilitate Upper Limb Function of Individuals with Acute to Subacute Cervical Spinal Cord Injury
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Restoring Motor and Sensory Hand Function in Tetraplegia Using a Neural Bypass System
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