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

NCT06672458 · ClinicalTrials.gov registry record · NA

Upper Extremity Functional Electrical Stimulation (FES) for Restoration of Upper Extremity Function After Spinal Cord Injury (SCI)

A NA study of Spinal Cord Injuries and Peripheral Nerve Injuries, sponsored by University of Miami.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT06672458: Recruiting NA study of Spinal Cord Injuries and Peripheral Nerve Injuries, sponsored by University of Miami.

NCT06672458 is a NA study of Spinal Cord Injuries and Peripheral Nerve Injuries that is actively recruiting participants, run by University of Miami. The registered enrollment target is 60 participants, roughly in line with the 61-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06672458, a NA study of Spinal Cord Injuries and Peripheral Nerve Injuries, is actively recruiting participants, sponsored by University of Miami.

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

Study Summary

The purpose of this research is to examine the effects that functional electrical stimulation (FES) therapy has on the way the arms, brain and spinal cord work. The study team wants to understand what recovery looks like in persons with a spinal cord injury (SCI) or peripheral nerve injury (PNI) using the MyndMove (MyndTec Inc., Ontario, Canada) therapy system. This type of therapy uses stimulation to help people with SCI and other neurological conditions to perform common tasks, work out, or strengthen muscles.

Primary Outcome

The Nine-Hole Peg Test assesses hand and finger dexterity. It is administered by asking the subject to take the pegs from a container, one by one, and place them into holes on the board as quickly as possible. Participants must then remove the pegs from the holes, one by one, and replace them back into the container. Test is performed at the beginning and end of each intervention visit. Scores are based on the time taken to complete the activity, recorded in seconds. (Only for subjects in short

Interventions

  • DEVICE MyndMove Short Term Therapy
  • OTHER Conventional Short Term Therapy
  • DEVICE MyndMove Long Term Therapy

Study Locations (1)

Florida

  • University of Miami - Miami Project to Cure Paralysis - Miami

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2024-11-01
Est. Completion 2029-01-31
Phase NA
University of Miami

721 total trials

What NCT06672458 shows while recruiting

NCT06672458 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, roughly in line with the 61-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target.

The record links to 2 conditions, with Spinal Cord Injuries appearing as the primary indexed condition, and to 3 interventions - of which MyndMove Short Term Therapy is the first listed.

NCT06672458 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT06672458 about?

NCT06672458 is a clinical study titled "Upper Extremity Functional Electrical Stimulation (FES) for Restoration of Upper Extremity Function After Spinal Cord Injury (SCI)". The purpose of this research is to examine the effects that functional electrical stimulation (FES) therapy has on the way the arms, brain and spinal cord work. The study team wants to understand what recovery looks like in persons with a spinal cord injury (SCI) or peripheral nerve injury (PNI) usi...

What is the current status of trial NCT06672458?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-11-01. Estimated completion is 2029-01-31.

What conditions does trial NCT06672458 study?

This clinical trial studies the following conditions: Spinal Cord Injuries, Peripheral Nerve Injuries.

What interventions are being tested in trial NCT06672458?

The interventions under investigation include: MyndMove Short Term Therapy (DEVICE), Conventional Short Term Therapy (OTHER), MyndMove Long Term Therapy (DEVICE).

Who is sponsoring clinical trial NCT06672458?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06672458 being conducted?

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

Similar trials for Spinal Cord Injuries

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 NCT06672458's enrollment target sits among peer trials

60 48th of 202 higher than 145 of 202 other Spinal Cord Injuries trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Spinal Cord Injuries 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT06358040 · started 2026-10 · NA

    Opioid Dispenser for Microdiscectomy/Laminectomy

Source: ClinicalTrials.gov NCT06672458, the US trial registry maintained by the National Library of Medicine. NCT06672458 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.