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Study identifier: NCT05305118 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

TSCS for Acute SCI

Condition: Acute Spinal Cord Injury · Blood Pressure · Hypotension  ·  Sponsor: Icahn School of Medicine at Mount Sinai

PhaseNA
Planned participants50
Who can joinAll sexes, 18 Years to 89 Years
Healthy volunteersNo

About this study

This project will focus on a novel approach to stabilizing blood pressure (BP) during inpatient rehabilitation after acute SCI. After SCI, people have unstable blood pressure, ranging from too low (orthostatic hypotension) to too high (autonomic dysreflexia). Unstable BP often interferes with performing effective physical rehabilitation after SCI. A critical need exists for the identification of safe, practical and effective treatment options that stabilize BP after traumatic SCI. Transcutaneous Spinal Cord Stimulation (TSCS) has several advantages over pharmacological approaches: (1) does not exacerbate polypharmacy, (2) can be activated/deactivated rapidly, and (3) can be applied in synergy with physical exercise. The study team is asking the key question: "What if applying TSCS earlier after injury could prevent the development of BP instability?" To facilitate adoption of TSCS for widespread clinical use, the study team plans to map and develop a parameter configuration that will result in an easy to follow algorithm to maximize individual benefits, while minimizing the burden on healthcare professionals. This project will provide the foundational evidence to support the feasible and safe application of TSCS in the newly injured population, thereby overcoming barriers to engagement in prescribed inpatient rehabilitation regimens that are imposed by BP instability.

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

Talk to the study team

Genevieve Curtis  ·  (617) 922-3141  ·  genevieve.curtis@mountsinai.org

Always discuss trial participation with your own doctor first.

Locations (1)

Mount Sinai Spinal Cord Injury Model SystemNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05305118