Actively Recruiting
Effect of the Stellate Ganglion Block on the Retinal Microcirculation
Led by University of Texas Southwestern Medical Center · Updated on 2025-11-19
50
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Surges in the sympathetic nervous system occur at the ictus of a variety of neurological critical illnesses including intracranial hemorrhage and ischemic stroke. It is hypothesized that these exaggerated increases in sympathetic nervous activity produce maladaptations that promote secondary brain injury. One of these possible mechanisms include diffuse vasospasm that cause cerebral ischemia. Hence, methods to abrogate the sympathetic nervous system in this context are under active investigation. One possible method is the regional anesthesia technique of the stellate ganglion nerve block, which is ordinarily used for complex regional pain syndrome, but has been shown to reduce cerebral sympathetic activity and reduces vasospasm in patients with subarachnoid hemorrhage. However, its effect on the microcirculation is not clear. Hence, we propose to study patients receiving the stellate ganglion nerve block as part of their standard medical care and to image their retinal microcirculation before and after the procedure using Optical Coherence Tomography Angiography (OCTA).
CONDITIONS
Official Title
Effect of the Stellate Ganglion Block on the Retinal Microcirculation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Patients receiving the stellate ganglion nerve block for an approved indication, e.g. complex regional pain syndrome
You will not qualify if you...
- Pregnancy
- Non-English speaking
- Temporary or permanent physical limitation that renders the patient unable to sit up and look inside OCTA device
AI-Screening
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Trial Site Locations
Total: 1 location
1
UT Southwestern Medical Center
Dallas, Texas, United States, 75235
Actively Recruiting
Research Team
N
Noah Jouett, DO, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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