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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 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.

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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.

Conditions Studied

Spinal Cord Injuries Blood Pressure SCI - Spinal Cord Injury Acute Spinal Cord Injury Blood Pressure Disorders Neuromodulation Spinal Cord Stimulation Traumatic Spinal Cord Injury

Interventions

  • DEVICE Digitimer

Study Locations (1)

New York

  • The Icahn School of Medicine at Mount Sinai - New York

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2022-01-01
Est. Completion 2026-10-01
Phase NA

Sponsor

Jill M. Wecht, Ed.D.

1 total trials

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What the Registry Record Tells You About NCT06000592

The ClinicalTrials.gov registry entry for NCT06000592 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 61-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (18% lower). The listed sponsor is Jill M. Wecht, Ed.D., which has 1 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

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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.