Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT04493372

Deciphering Preserved Autonomic Function After Spinal Cord Injury

Led by Mayo Clinic · Updated on 2026-05-01

69

Participants Needed

1

Research Sites

303 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study looks to characterize gradients of dysfunction in the autonomic nervous system after spinal cord injury. The autonomic nervous system plays key roles in regulation of blood pressure, skin blood flow, and bladder health- all issues that individuals with spinal cord injury typically suffer. Focusing on blood pressure regulation, the most precise metric with broad clinical applicability, the investigators will perform laboratory-based tests to probe the body's ability to generate autonomic responses. For both individuals with spinal cord injury and uninjured controls, laboratory-based experiments will utilize multiple parallel recordings to identify how the autonomic nervous system is able to inhibit and activate signals. The investigators anticipate that those with autonomic dysfunction after spinal cord injury will exhibit abnormalities in these precise metrics. The investigators will further have research participants wear a smart watch that tracks skin electrical conductance, heart rate, and skin temperature, which can all provide clues as to the degree of autonomic dysfunction someone may suffer at home. The investigators will look to see if any substantial connections exist between different degrees of preserved autonomic function and secondary autonomic complications from spinal cord injury. In accomplishing this, the investigators hope to give scientists important insights to how the autonomic nervous system works after spinal cord injury and give physicians better tools to manage these secondary autonomic complications.

CONDITIONS

Official Title

Deciphering Preserved Autonomic Function After Spinal Cord Injury

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 50 years old
  • Adult onset, traumatic spinal cord injury for participants with spinal cord injury
  • American Spinal Injury Association Impairment Scale A-D to include a range of autonomic dysfunction
  • Neurological level of injury from C1 to T12 as defined by standard classification
Not Eligible

You will not qualify if you...

  • History of cardiovascular disease, hypertension, neurologic disorders (except spinal cord injury), or diabetes
  • Pregnant or lactating women
  • Currently taking blood thinners
  • Presence of pacemaker, implanted defibrillator, or intrathecal pump incompatible with MRI
  • Cognitive issues preventing informed consent
  • Body mass index over 30 kg/m2 for control participants to limit cardiovascular and diabetes effects

AI-Screening

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Trial Site Locations

Total: 1 location

1

Mayo Clinic

Rochester, Minnesota, United States, 55902

Actively Recruiting

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Research Team

P

PI

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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