ClinicalTrials.gg
RecruitingNCT05288790META HIV CVDUpdated Aug 27, 2026

Microbiome Metabolites and Alcohol in HIV to Reduce CVD RCT

A Phase 2 interventional study of Probiotic and Placebo in Microtia, Dysbiosis and Alcohol Drinking, sponsored by Vanderbilt University Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years to 89 Years. Per ClinicalTrials.gov, last updated 2026-08-27.

Sponsored by Vanderbilt University Medical Center · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2023; still recruiting 3 years 1 month later.
Phase
Phase 2
Study type
Interventional
Enrollment
250
Allocation
Randomized
Ages
18 Years to 89 Years
Sex
All
01

Study summary

Among people living with HIV, heavy drinking increases the risk of heart disease and death. Studies suggest that alcohol changes the number and kind of bacteria in your gut and these changes increase the risk of heart disease and death. This randomized controlled trial will determine whether a pill containing healthy gut bacteria can increase the number good bacteria in the gut, lower levels of inflammation, and lower the risk of heart disease and death.

Read the detailed description

Among people living with HIV (PLWH), heavy drinking increases the risk of cardiovascular disease (CVD) and death. Data suggest that alcohol-associated gut dysbiosis partially drives this risk. Whether interventions targeting alcohol-associated gut dysbiosis among PLWH improve dysbiosis, lower levels of microbial translocation, inflammation, and harmful metabolites (e.g., trimethylamine N-oxide [TMAO)]) is unknown. The investigators' hypothesis for this P01 application is that among PLWH, a probiotic can mitigate or reduce alcohol associated gut dysbiosis and lower levels of microbial translocation, inflammation, and improve metabolite profiles (Project 1); and that harmful levels of these metabolites will be associated with higher CVD and death risk (Project 2). This team, with expertise in alcohol, HIV, gut microbiome, and biomarker research has conducted two NIAAA funded trials, a metabolite study, and a gut microbiome study among Russian PLWH who are heavy drinkers. Data from these studies show that among PLWH: (1) heavy drinking is associated with incident CVD, death and gut dysbiosis (characterized by a reduction in butyrate producing bacteria); and (2) this gut dysbiosis is associated with inflammation, altered bile acids, and high TMAO levels. Given these data and reports from pilot studies showing that probiotics are safe, may improve gut dysbiosis and reduce inflammation among PLWH, the investigators propose an RCT among 250 PLWH with heavy alcohol consumption who are on antiretroviral therapy and have CD4+ counts≥350 cells/mm3 to compare the effects of a probiotic tailored to alcohol associated gut dysbiosis vs. placebo to: (1) improve GI dysbiosis; (2) reduce plasma metabolite (e.g., TMAO) and biomarker levels of microbial translocation and inflammation; and (3) lower CVD and mortality risk. All participants will receive evidenced-based counseling for alcohol use. The specific aims will compare the effects of a tailored probiotic vs. placebo at 6 months on (Aim 1) dysbiosis (fecal Firmicutes to Bacteroidetes (F/B) ratio, primary study outcome; fecal Lachnospiraceae-family of butyrate producers) and plasma metabolites (plasma butyrate, deoxycholic acid:cholic acid ratio, and TMAO) (Aim 2) biomarkers of inflammation plasma, IL-6, D-dimer, sCD14), microbial translocation [Lipopolysaccharide binding protein], (Aim 3) cardiovascular risk (Reynolds risk score), mortality risk (VACS index); (Aim 4 exploratory) alcohol consumption (% heavy drinking days in past month) and HIV disease progression (CD4 cell count). The investigators hypothesize that as compared with placebo, the probiotic arm will have significantly: (1) higher F/B ratio and levels of fecal Lachnospiraceae, plasma butyrate, deoxycholic acid: cholic acid ratio and lower levels of TMAO; (2) lower plasma biomarker levels of microbial translocation and inflammation; (3) lower Reynolds risk score and VACS index; (4) lower % heavy drinking days in the past month and higher CD4 cell counts. The findings from this RCT, Microbiome, mETabolites, and Alcohol in HIV to reduce CVD (META HIV CVD RCT), will inform probiotics' role as standard adjunctive therapy complementing alcohol interventions among PLWH who are heavy drinkers.

02

Conditions studied

  • Microtia
  • Dysbiosis
  • Alcohol Drinking
  • HIV Infections
  • Cardiovascular Diseases
03

In context

Congenital Microtia

33 studies on the registry are indexed under Congenital Microtia; 10 are open to participants now.

This study's planned enrollment of 250 is above the median of 34 across 23 interventional studies indexed under Congenital Microtia.

Browse Congenital Microtia studies →

Lead sponsor

Vanderbilt University Medical Center is the lead sponsor of 833 studies on the registry; 155 are open to participants now.

Of its 125 completed or terminated interventional studies of FDA-regulated products, 92 (74%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 89 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • infected

Exclusion criteria

Exclusion Criteria:

  • Not fluent in English
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
250 participants (estimated)

Study arms

  • Experimental
    Study Supplement

    Probiotic

    Dietary Supplement: Probiotic

  • Placebo comparator
    Study placebo

    Placebo

    Dietary Supplement: Placebo

Interventions

  • Dietary supplementProbiotic

    Dietary supplement

  • Dietary supplementPlacebo

    Placebo sachet

06

What researchers measure

Primary outcomes

  1. Firmicutes to Bacteroidetes ratio

    Dysbiosis

    Time frame: 6 months

Secondary outcomes

  1. Intestinal permeability

    measuring levels of butyrate, deoxycholic acid:cholic acid ratio, and TMAO

    Time frame: 6, 12 months

  2. Firmicutes to Bacteroidetes ratio

    Dysbiosis measurement

    Time frame: 12 months

  3. Microbial Translocation

    measuring plasma lipopolysaccharide binding protein

    Time frame: 6, 12 months

  4. Inflammation

    measuring plasma for interleukin 6 \[IL-6\], D-dimer, and sCD14

    Time frame: 6, 12 months

Other outcomes

  1. Mortality

    Veterans Aging Cohort Study Index Score (lower scores are better and higher scores are worse) (ranges from 0-164)

    Time frame: 6 and 12 months

  2. CVD risk

    Reynolds Risk Score (the higher the score the higher the risk) (ranges from 100-400 mg/dL)

    Time frame: 6 and 12 months

07

Study locations

1 of 1 sites recruiting
  • Vanderbilt University Medical Center
    Nashville, Tennessee 37232, United States
    Recruiting
    • David Crenshaw, MSW · Contact615-322-7343
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05288790
Responsible party
Matthew S.Freiberg (Professor of Medicine, Vanderbilt University Medical Center) — Principal investigator
First posted
Mar 21, 2022
Start date
Sep 18, 2023
Primary completion
Mar 31, 2027 (estimated)
Completion
Aug 31, 2027 (estimated)
Last update
Aug 27, 2026

Study contacts

Grace Wallace, BS
Contact
grace.wallace@vumc.org
615-936-5356
Emily Smith, MPH
Contact
emily.k.smith@vumc.org
6158757253

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Probiotic

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