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Study identifier: NCT06903078 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study That Collects Participant Data and Biospecimens to Analyze Pathogenic Exosomes That Mediate Increased Vascular Dementia Risk in Individuals With Herpes Zoster.

Condition: Herpes Zoster (HZ) · Vascular Dementia  ·  Sponsor: Center for Clinical Studies, Texas

PhaseN/A
Planned participants375
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The purpose of this observational research study is to study if patients with herpes zoster, also known as Shingles, have a higher risk of vascular dysfunction (problems with blood vessels, including stroke) and vascular dementia (problems with mental decline as a result of decreased blood flow to the brain) compared to patients without herpes zoster. Patients are evaluated based on the group they are assigned too: 1. Herpes Zoster (HZ) Group: individuals presenting with untreated herpes zoster. These participants will have 6 visits: * Day 1 = 1st day presenting to clinic with acute zoster * 7 days post zoster * 1 month after Day 1 * 3 months after Day 1 * 6 months after Day 1 * 12 months after Day 1 2. Control Group: individuals without herpes zoster o Day 1 (only 1 visit will be completed) This study does not have a study medication/device. Standard of care for all patients will be followed.

This description comes directly from the study's public registry record.

Talk to the study team

Study Principal Investigator  ·  281-333-2288  ·  info@ccstexas.com

Director of Research  ·  281-333-2288  ·  dyetman@ccstexas.com

Always discuss trial participation with your own doctor first.

Locations (2)

Center for Clinical Studies, LTD. LLPHouston, Texas, United StatesRecruiting
Center for Clinical Studies, LTD. LLPWebster, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06903078