RecruitingNot ApplicableNCT06000592

Safety, Feasibility, and Efficacy of TSCS on Stabilizing Blood Pressure for Acute Inpatients With SCI

Safety, Feasibility, and Efficacy of Transcutaneous Spinal Cord Stimulation on Stabilizing Blood Pressure for Acute Inpatients With Spinal Cord Injury


Sponsor

Jill M. Wecht, Ed.D.

Enrollment

50 participants

Start Date

Jan 1, 2022

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 14 YearsMax Age: 100 Years

Inclusion Criteria7

  • Newly injured patients with traumatic SCI
  • Admitted to Acute Inpatient Rehabilitation at Mount Sinai
  • Within one year of SCI
  • Seated hypotension (systolic BP ≤ 110 mmHg for males or ≤ 100 mmHg for females)
  • Orthostatic hypotension (fall in systolic BP ≥ 20 mmHg and/or a fall in diastolic BP ≥ 10 mmHg within 10 minutes of assuming an upright position)
  • Daily fluctuation in systolic BP ≥ 20 mmHg and/or fluctuation in diastolic BP ≥ 10 mmHg
  • At least 14 years old

Exclusion Criteria10

  • Implanted brain/spine/nerve stimulators
  • Cochlear implants
  • Cardiac pacemaker/defibrillator, or intracardiac lines
  • Open skin lesions on or near the electrode placement sites (neck, upper back)
  • Significant coronary artery or cardiac conduction disease
  • Recent history of myocardial infarction
  • Insufficient mental capacity to understand and independently provide consent
  • Pregnancy
  • Cancer
  • Deemed unsuitable by study physician

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICEDigitimer

transcutaneous spinal cord stimulation for blood pressure control following spinal cord injury.


Locations(1)

The Icahn School of Medicine at Mount Sinai

New York, New York, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06000592


Related Trials