Gut health fix for HIV fatty liver? early trial tests probiotics
NCT ID NCT06113003
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-phase study tests whether taking prebiotic fiber and probiotics can improve fatty liver disease in people with HIV. Researchers believe changes in gut bacteria may contribute to liver problems. The trial involves 63 participants and measures liver fat and gut health markers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Wheat dextrin fiber (prebiotic) and probiotic packet
- What this could lead to
- If it works, this could point toward a simple dietary supplement approach to help manage fatty liver disease in people with HIV.
- What could go wrong
- This is a very early, small study (63 participants) testing only short-term markers, not long-term health outcomes. The supplements may not produce meaningful improvement.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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63 people
The number who actually took part.
- Started
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Apr 2024
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 89 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * One of the following: 1. One or more of the components of metabolic syndrome, defined as: 1. Diagnosis of diabetes: on medication for diabetes for at least 6 months, HbA1c \>6.5%, or fasting glucose \>99 mg/dL 2. Elevated fasting triglycerides: \>149 mg/dL or on medication for dyslipidemia 3. Reduced HDL-C: \<40 mg/dL in males, \<50 mg/dL in females or on medication for dyslipidemia 4. Elevated blood pressure: \>129 mm Hg systolic and/or \>84 mm Hg diastolic or on medication for hypertension 5. Prior diagnosis of hepatic steatosis or NAFLD: hepatic steatosis noted on interpretation of clinical imaging, CT scan liver density of less than 58 HU, Fibroscan CAP score \>238 dB/m, MRI-PDFF ≥5%, liver biopsy showing ≥5% triglyceride content 2. Persistently abnormal transaminases: elevated liver enzymes defined by transaminases ≥1.5 upper limit of normal (\[ULN\] = 35 IU/mL) and/or gammaglutamyltransferase level ≥2 ULN (ULN = 60 IU/L) on 2 blood samples within at least a 3-month interval 3. BMI ≥ 30 kg/m2 * Documented HIV infection * On antiretroviral therapy for at least 18 months * HIV-1 RNA \<50 copies/ml for the prior 12 months * CD4 count \>350 cells/microliter for the prior 12 months * Ability to be contacted by phone (home or cell) * Access to a private (i.e. accessible only to participant and immediate family or roommates) refrigerator for 6 months * Able and willing to comply with all study protocols and procedures Exclusion Criteria: * Not fluent in English * Known allergy to the study product or its formulation * Pregnant or planning to become pregnant within the next six months * History of chronic diarrhea in the past three months * Breastfeeding * History of celiac disease * Prior diagnosis of non-NAFLD liver disease including, but not limited to, Wilson Disease, hemochromatosis, autoimmune hepatitis, primary biliary cirrhosis, primary sclerosing cholangitis, and alpha 1 antitrypsin deficiency * On medications associated with secondary NAFLD including systemic corticosteroids, tamoxifen, methotrexate, nifedipine, history of cancer chemotherapy, * Positive hepatitis C quant or on treatment for hepatitis C within the last 12 months * History of cirrhosis or liver transplant * AUDIT-C score ≥3 women and ≥4 in men * History of inflammatory bowel disease * History of all other GI surgery within the past 12 months * Use of antibiotics in the past 30 days * Metal shrapnel, MRI incompatible hardware or claustrophobia that would preclude MRI imaging * Inability to participate in the study in the opinion of the participant's HIV treatment provider * Use of prebiotic(s) including fiber supplements and/or probiotic(s) within the past 90 days * Participant has history of hemicolectomy, colectomy, small bowel resection, bariatric surgery, gastric bypass surgery, or short bowel syndrome
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Vanderbilt University Medical Center
Nashville, Tennessee, 37232, United States
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