Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Mayo Clinic
Rochester, Minnesota, United States, 55902
Actively Recruiting
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
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here