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Recruiting NCT07210437

Longitudinal Autonomic Characterization as a Predictor for Secondary Medical Complications Post-SCI

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Plain-language summary for patients

Trial Parameters

Condition Spinal Cord Injuries
Sponsor Mayo Clinic
Study Type INTERVENTIONAL
Phase N/A
Enrollment 18
Sex ALL
Min Age 18 Years
Max Age 75 Years
Start Date 2026-01-31
Completion 2027-12-31
Interventions
Tests of sympathetic inhibitionTests of above level sympathetic activationTesting of below level sympathetic activation

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Brief Summary

The purpose of this research is to learn about how the body is able to balance changes in blood pressure, how that changes over time, and how these changes impact a participant's risk of developing medical problems.

Eligibility Criteria

Inclusion criteria * 18-75 years old * Spinal cord injury with neurological level of injury from C6-T12 * ASIA Impairment Scale A-D. * Either acute SCI \<3 months prior (n=10) or chronic SCI (\>1 year since injury, n=8). Exclusion criteria * Symptoms of cardiovascular (including, but not limited to: hypertension, stroke, chest pain, etc.), respiratory, peripheral neurological or autonomic disease (particularly diabetes mellitus requiring treatment); * Women who are pregnant or lactating * Taking or being administered a medication known to potentially have adverse interactions with phenylephrine * In the judgement of the principal investigator, any illness or condition that will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results.

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