Madison, WINCT05820893Now EnrollingIRB Ready

Gulf War Illness Clinical Trial in Madison, WI

Access cutting-edge gulf war illness treatment through this phase 2 clinical trial at a research site in Madison. Study-provided care at no cost to qualified participants.

Sponsored by VA Office of Research and Development

Quick Self-Assessment

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Expert Care in Madison

Access gulf war illness specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related gulf war illness treatment provided free

Apply for This Madison Location

Check if you qualify for this gulf war illness clinical trial in Madison, WI

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Madison

    Convenient for WI 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 Madison site if eligible
  4. 4Begin participation

About This Gulf War Illness Study in Madison

Gulf War Illness (GWI) affects an estimated 25-32% of the over 700,000 coalition troops deployed to the Persian Gulf as part of the First Gulf War. GWI causes a range of pain, fatigue, gastrointestinal, skin, neurologic, and respiratory symptoms. New treatments to reduce GWI-associated morbidity are critically needed. Research suggests a role for the gastrointestinal microbiome in mediating health, including through impacting metabolism and immunity. The disruption of this microbiome plays a role in multiple diseases, and preliminary data suggest that Veterans with GWI have altered gut microbiota. The investigators will evaluate the effectiveness of a dietary fiber prebiotic supplement intervention on improving the quality of life of Veterans with GWI.

Sponsor: VA Office of Research and Development

Who Can Participate

Inclusion Criteria

Ability to provide informed written consent
Willing to comply with all study procedures and be available for the duration of the study (including providing stool samples)
Meeting the modified Kansas GWI case definition\
with gut symptoms endorsed
Deployed to Persian Gulf during Operations Desert Storm or Desert Shield56.Aged 50-85 years old
Moderate to severe GWI symptoms lasting at least 6 months in a minimum of three of the six symptom domains (one of which must be fatigue). The symptom domains are:
Pain (joint pain, muscle pain)
Gastrointestinal (diarrhea, nausea, vomiting, cramping)
Respiratory (persistent cough, wheezing)
Skin (rashes)
Fatigue (sleep problems, fatigue)
Neurologic (memory problems, headaches, dizziness, mood changes)

Exclusion Criteria

A Known SARS-CoV-2 infection in the last 60 days and/or with a diagnosis of post-acute sequelae of COVID-19 (PASC, sometimes called long COVID) defined as COVID-19 symptoms lasting for greater than 6 months.
Subjects identified as, or appearing to, lack consent capacity
Alcohol abuse (greater than 14 drinks per week for men and 7 drinks per week for women)
Use of investigational drugs, biologics, or devices within 30 days prior to randomization.
Individuals who are pregnant, lactating or planning on becoming pregnant during the study.
Diagnosed inflammatory bowel disease, Crohn's disease, or Celiac's disease
Uncontrolled/untreated hypothyroidism
Previous gastrointestinal surgery (colorectal surgery, gastric bypass, intestinal resection)
Systemic antibiotics in the last 30 days
Fecal microbiota transplant in the last 30 days
Active dysphagia
Allergies to any of the ingredients in MSPrebiotic
Use of immunomodulatory medications in the last 30 days
Any other factor, condition, or medication not listed above the Investigators believe will affect the response in the gut or the interpretation of results.

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 Madison?

Yes, this clinical trial (NCT05820893) has an active research site in Madison, WI 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.

Gulf War Illness Treatment Options in Madison, WI

If you're searching for gulf war illness treatment options in Madison, WI, this clinical trial (NCT05820893) 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 Madison research site is actively enrolling participants for this phase 2 clinical trial. You'll receive care from experienced gulf war illness 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 gulf war illness clinical trials near you to find additional studies recruiting in your area.

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