Webster, TXNCT06903078Now EnrollingIRB Ready

Herpes Zoster (HZ) Clinical Trial in Webster, TX

Access cutting-edge herpes zoster (hz) treatment through this clinical trial at a research site in Webster. Study-provided care at no cost to qualified participants.

Sponsored by Center for Clinical Studies, Texas

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Expert Care in Webster

Access herpes zoster (hz) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related herpes zoster (hz) treatment provided free

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Check if you qualify for this herpes zoster (hz) clinical trial in Webster, TX

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Why Participate?

  • No-Cost Study Care

  • Local to Webster

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Webster site if eligible
  4. 4Begin participation

About This Herpes Zoster (HZ) Study in Webster

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.

Sponsor: Center for Clinical Studies, Texas

Who Can Participate

Inclusion Criteria

At the Screening Visit (Visit 1/Day 1), all participants must meet all the following criteria in order to be considered for participation in the study:
Be a male or female ≥ 18 years of age.
Present to clinic for routine dermatologic evaluation with or without rash.
Are willing and able to complete study visits and procedures, and able to effectively communicate with the investigator and other study personnel.
Have adequate venous access and are willing to undergo venipuncture for blood draws.
Able to provide written informed consent prior to any study procedures. Additional inclusion criteria for Herpes zoster (HZ) participants,
Present with acute, vesicle-stage HZ that has not been treated with antiviral therapies
Are willing and have reliable transportation to complete additional follow-up visits at 7 days, 1 month, 3 months, 6 months, and 12 months after initial visit for acute HZ.

Exclusion Criteria

At the Screening Visit (Visit 1/Day 1), participants meeting any of the following criteria will be excluded from participation in the study:
Female individuals who are pregnant or breast-feeding.
Receiving systemic or topical antivirals for varicella zoster virus (VZV).
Sensitivity or allergy to systemic or topical antiviral medications for HZ.
History of diagnosed HZ within the last 8 years.
Received a HZ vaccine (e.g., Zostavax®/Shingrix®) within the last 8 years.
Received any vaccinations within the last 3 months.
Currently taking immunosuppressive therapies, including medications and radiation.
Currently taking any anticoagulants.
History of any coagulation disorder(s).
History of end-stage renal disease or uremia.
History of end-stage liver disease.
History of HIV.
Have had a COVID-19 infection in last 3 months.
Any history of non-skin cancers within the last 3 months.
History of serious infection requiring hospitalization in the last 3 months.
Prior history of cardiovascular accident or myocardial infarction within the last 12 months.
Prior cerebrovascular accident in the past 12 months.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Webster?

Yes, this clinical trial (NCT06903078) has an active research site in Webster, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Herpes Zoster (HZ) Treatment Options in Webster, TX

If you're searching for herpes zoster (hz) treatment options in Webster, TX, this clinical trial (NCT06903078) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Webster research site is actively enrolling participants for this clinical trial. You'll receive care from experienced herpes zoster (hz) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all herpes zoster (hz) clinical trials near you to find additional studies recruiting in your area.

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