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NCT06000592 · ClinicalTrials.gov registry record · NA
Safety, Feasibility, and Efficacy of TSCS on Stabilizing Blood Pressure for Acute Inpatients With SCI
A NA study of Spinal Cord Injuries and Blood Pressure, sponsored by Jill M. Wecht, Ed.D..
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT06000592: Recruiting NA study of Spinal Cord Injuries and Blood Pressure, sponsored by Jill M. Wecht, Ed.D..
NCT06000592 is a NA study of Spinal Cord Injuries and Blood Pressure that is actively recruiting participants, run by Jill M. Wecht, Ed.D.. The registered enrollment target is 50 participants, below the 61-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (18% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06000592, a NA study of Spinal Cord Injuries and Blood Pressure, is actively recruiting participants, sponsored by Jill M. Wecht, Ed.D..
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
Current forms of pharmacologic and non-pharmacologic treatments for hypotension and orthostatic hypotension (OH) remain inadequate during acute inpatient rehabilitation (AIR) following a traumatic spinal cord injury (SCI). A critical need exists for the identification of safe, practical, and effective treatment options that stabilize blood pressure (BP) after traumatic SCI. Recent published evidence suggests that transcutaneous Spinal Cord Stimulation (TSCS) can be used to raise seated BP, and mitigate the falls in BP during orthostatic repositioning in individuals with chronic SCI. This site-specific project will focus on the use of TSCS to stabilizing seated BP and mitigate the fall in BP during orthostatic repositioning during AIR following traumatic SCI.
Primary Outcome
Blood pressure changes (mmHg) during the sit-up test with TSCS compared to no stimulation.
Conditions Studied
Interventions
- DEVICE Digitimer
Study Locations (1)
New York
- The Icahn School of Medicine at Mount Sinai - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2022-01-01 |
| Est. Completion | 2026-10-01 |
| Phase | NA |
What NCT06000592 shows while recruiting
NCT06000592 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 61-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (18% lower).
The record links to 8 conditions, with Spinal Cord Injuries appearing as the primary indexed condition, and to 1 intervention - of which Digitimer is the first listed.
NCT06000592 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT06000592 about?
NCT06000592 is a clinical study titled "Safety, Feasibility, and Efficacy of TSCS on Stabilizing Blood Pressure for Acute Inpatients With SCI". Current forms of pharmacologic and non-pharmacologic treatments for hypotension and orthostatic hypotension (OH) remain inadequate during acute inpatient rehabilitation (AIR) following a traumatic spinal cord injury (SCI). A critical need exists for the identification of safe, practical, and effecti...
What is the current status of trial NCT06000592?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2022-01-01. Estimated completion is 2026-10-01.
What conditions does trial NCT06000592 study?
This clinical trial studies the following conditions: Spinal Cord Injuries, Blood Pressure, SCI - Spinal Cord Injury, Acute Spinal Cord Injury, Blood Pressure Disorders.
What interventions are being tested in trial NCT06000592?
The interventions under investigation include: Digitimer (DEVICE).
Who is sponsoring clinical trial NCT06000592?
This trial is sponsored by Jill M. Wecht, Ed.D., which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06000592 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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 NCT06000592's enrollment target sits among peer trials
50 59th of 202 higher than 141 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
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