Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07210411

Acute and Chronic Repercussion of Spinal Cord Stimulation After Spinal Cord Injury

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this research is to learn about how the participant's body is able to balance changes in blood pressure, and how spinal cord stimulation affects these changes as well as immune \& cardiovascular function in participants with spinal cord injury.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTTests of sympathetic inhibitionBolus phenylephrine infusion using the Oxford technique will generate the need to inhibit sympathetic activity. Similarly, resting state Mayer waves will be assessed with regard to heart rate and blood pressure responses.
DIAGNOSTIC_TESTTests of above level sympathetic activationCold pressor test of the hand will be used to cause sympathetic activation. Valsalva's maneuver will assess the ability to buffer against blood pressure fall (phase II).
DIAGNOSTIC_TESTTesting of below level sympathetic activationCold pressor test of the foot and bladder pressor response (in individuals with SCI) will be tested.
DEVICEEpidural stimulationCurrently implanted epidural stimulation will be used during diagnostic testing.
DEVICETranscutaneous stimulationTranscutaneous stimulation will be used for participants with spinal cord injury without an implanted stimulator during diagnostic testing.

Timeline

Start date
2026-03-05
Primary completion
2030-12-31
Completion
2031-04-01
First posted
2025-10-07
Last updated
2026-03-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07210411. Inclusion in this directory is not an endorsement.