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
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Tests of sympathetic inhibition | Bolus 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_TEST | Tests of above level sympathetic activation | Cold 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_TEST | Testing of below level sympathetic activation | Cold pressor test of the foot and bladder pressor response (in individuals with SCI) will be tested. |
| DEVICE | Epidural stimulation | Currently implanted epidural stimulation will be used during diagnostic testing. |
| DEVICE | Transcutaneous stimulation | Transcutaneous 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.