Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02037620 · ClinicalTrials.gov registry record · NA
Recovery of Cardiovascular Function With Epidural Stimulation After Human Spinal Cord Injury
A NA study of Spinal Cord Injury, sponsored by University of Louisville.
- Completed
- Registry status
- NA
- Development phase
- 5
- Enrollment target
- 1
- Study location
NCT02037620: Completed NA study of Spinal Cord Injury, sponsored by University of Louisville.
NCT02037620 is a NA study of Spinal Cord Injury that has completed, run by University of Louisville. The registered enrollment target is 5 participants, below the 86-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02037620, a NA study of Spinal Cord Injury, has completed, sponsored by University of Louisville.
- COMPLETED
- Registry status
- NA
- Development phase
- 5 participants
- Enrollment target
- 1
- Study location
Study Summary
We propose to demonstrate that epidural stimulation (ES) can be used to recover significant levels of autonomic control of cardiovascular and respiratory function as well as the ability to voluntarily control leg movements below the injury level. This intervention would provide an immediate therapeutic alternative to individuals who now have no recourse for treatment.
Primary Outcome
Noninvasive continuous blood pressure measured from a finger cuff by plethysmographic technique (Finometer Pro, FMS, Amsterdam, Netherlands) was calibrated to brachial blood pressure. Mean arterial pressure was calculated as one-third of systolic blood pressure plus two-third of diastolic blood pressure.
Conditions Studied
Interventions
- DEVICE 5-6-5 Specify electrode
- DEVICE Restore Advance Pulse Generator
Study Locations (1)
Kentucky
- University of Louisville - Louisville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2014-07 |
| Est. Completion | 2019-09-20 |
| Phase | NA |
What the finished NCT02037620 record still lists
NCT02037620 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 86-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (94% lower).
The record links to 1 condition, with Spinal Cord Injury appearing as the primary indexed condition, and to 2 interventions - of which 5-6-5 Specify electrode is the first listed.
NCT02037620 reports a single indexed study location in Kentucky.
Frequently Asked Questions
What is clinical trial NCT02037620 about?
NCT02037620 is a clinical study titled "Recovery of Cardiovascular Function With Epidural Stimulation After Human Spinal Cord Injury". We propose to demonstrate that epidural stimulation (ES) can be used to recover significant levels of autonomic control of cardiovascular and respiratory function as well as the ability to voluntarily control leg movements below the injury level. This intervention would provide an immediate therapeu...
What is the current status of trial NCT02037620?
This trial is currently completed. It is a NA study. The enrollment target is 5 participants. The study started on 2014-07. Estimated completion is 2019-09-20.
What conditions does trial NCT02037620 study?
This clinical trial studies the following conditions: Spinal Cord Injury.
What interventions are being tested in trial NCT02037620?
The interventions under investigation include: 5-6-5 Specify electrode (DEVICE), Restore Advance Pulse Generator (DEVICE).
Who is sponsoring clinical trial NCT02037620?
This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02037620 being conducted?
This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for 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.
Where NCT02037620's enrollment target sits among peer trials
5 96th of 99 higher than 3 of 99 other Spinal Cord Injury trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Spinal Cord Injury 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
-
Cortical Recording and Stimulating Array Brain-Machine Interface
RECRUITING · NA
-
Clinical Outcome Assessment for AT & BCI
RECRUITING · NA
-
Motoneuron Recruitment and Motor Evoked Potential Up-Conditioning (MEP) in Spinal Cord Injury (SCI)
RECRUITING · NA
-
SCI&U Peer Health Coaching Program for Individuals Newly Discharged From Inpatient Rehabilitation
RECRUITING · NA
-
At-Home Genital Nerve Stimulation for SCI Bowel
RECRUITING · NA
-
Exoskeleton and Spinal Cord Stimulation for SCI
RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia