Studying How Stellate Ganglion Block Affects Retinal Blood Flow in Adults
Led by University of Texas Southwestern Medical Center · Updated on 2025-11-19
50
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Researchers are investigating the effects of the stellate ganglion nerve block on retinal microcirculation in patients with neurological critical illnesses such as intracranial hemorrhage and subarachnoid hemorrhage. These conditions often cause surges in the sympathetic nervous system that may lead to secondary brain injury through mechanisms like diffuse vasospasm and cerebral ischemia. The study aims to understand how blocking the sympathetic nervous system might influence microcirculation in the eye.
Participants in this observational study will receive the stellate ganglion nerve block as part of their standard medical care. The key procedure involves imaging the retinal microcirculation using Optical Coherence Tomography Angiography OCTA before and after the nerve block. This technique is known to reduce cerebral sympathetic activity and vasospasm, and the study will assess its impact on retinal blood vessel density and perfusion.
During the study, participants will undergo OCTA scans to measure vascular and perfusion density one day after the procedure. Researchers will monitor these changes to evaluate the nerve blocks effect on retinal microcirculation. The study is sponsored by the University of Texas Southwestern Medical Center and will include adult patients receiving this nerve block for approved conditions. Participation involves imaging and standard care without additional interventions, and the study is expected to conclude by October 2026.
CONDITIONS
Brief Title
Effect of the Stellate Ganglion Block on the Retinal Microcirculation
Research Team
N
Noah Jouett, DO, PhD
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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
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Implementation
Duration - 1 day
Participants undergo Optical Coherence Tomography Angiography scans before and after receiving the stellate ganglion nerve block.
2 visits (in-person)
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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Published Research Related To This Trial
Retinal vascular image analysis as a potential screening tool for cerebrovascular disease: a rationale based on homology between cerebral and retinal microvasculatures.