← Eichor
Study identifier: NCT06841198 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Cardiovascular Function and Response to Stimulation Within the First Year After Spinal Cord Injury

Condition: Spinal Cord Injuries (SCI) · Orthostatic Hypotension, Dysautonomic · Cardiovascular  ·  Sponsor: Kessler Foundation

PhaseNA
Planned participants15
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersYes

About this study

The study aims to explore how cardiovascular function changes in the first year after a spinal cord injury, and to see how different treatments, like spinal stimulation through the skin (transcutaneous spinal stimulation), affect blood pressure. The main questions are: How does stimulation affect blood pressure over the year? What is the level of cardiovascular activation throughout the year? The study will start during the inpatient stay at the Kessler Institute for Rehabilitation and continue after discharge as an outpatient, totaling about 20-29 sessions over the year.

This description comes directly from the study's public registry record.

Talk to the study team

Leighann Martinez, BA  ·  (973)324-3557  ·  lmartinez@kesslerfoundation.org

Always discuss trial participation with your own doctor first.

Locations (1)

Kessler FoundationWest Orange, New Jersey, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06841198