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Enrolling by invitation NCT07052409

Developing Interventions for Protecting HIV-Exposed Uninfected Infants Against Severe Infections

No phase Interventional Gut Microbiome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Inkomazi.
Who it may be relevant to
Registry conditions: Gut Microbiome. Basic parameters: 6 months — 45 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Africa
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Research has shown that babies who are exposed to HIV, but are uninfected (negative HIV status), have a bigger risk of developing severe infections. There are naturally occurring organisms in the gut that may determine how the body protects itself against infections. These organisms may be different in babies who were exposed to the HIV virus in utero, compared to those who were not exposed. This study wants to see if the organisms in the gut of babies can be modified by supplementing the diet of the pregnant mother or of the baby at 6 months of age with Inkomasi (pasteurized fermented milk). The study will compare the type and amount of organisms in those who received supplementation and those who did not receive supplementation.

Detailed description

1. The study will enroll 24 pregnant women with HIV at 36 weeks gestational age and randomize them 1:1 to receive 500 ml daily of pasteurized fermented milk (Inkomasi) or not. Changes in maternal gut microbiota from enrollment to 2-4 weeks postpartum will be compared between groups. The study will also compare the gut microbiome at infants born to mothers who received Inkomasi with those born to mothers who did not receive Inkomasi. 2. The study will enroll 24 HIV-exposed uninfected infants (HEU) at 24 weeks of age and randomize them 1:1 to receive ≥15 ml daily of pasteurized fermented milk (Inkomasi) or not. Changes in infant gut microbiota from enrollment to 4 weeks after enrollment will be compared between groups.

Interventions

  • Dietary supplement Inkomazi
    Pasteurized fermented milk

Primary outcome measures

  • Infant gut microbiome [Time frame: from enrollment to 4-10 weeks after enrollment]
  • Maternal gut microbiome [Time frame: 4-10 weeks after initiation of the intervention]

Eligibility criteria

Inclusion criteria

  • Pregnant women with HIV HIV-exposed uninfected infants

Exclusion criteria

\-

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

South Africa · 1 center
  • Witwatersrand — Johannesburg

Identifiers

NCT: NCT07052409 · 24-1383 COMIRB

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗