HIV and Changes in the Gut Microbiome After Changes in Antiretroviral Therapy (ART)

Sponsor
University of Manchester (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06100211
Collaborator
(none)
15
11

Study Details

Study Description

Brief Summary

This is a study that aims to contribute to our understanding of how antiretroviral therapy effects the gut microbiome which, if known, could inform decisions about drug choices at an individual level.

Our gut health is extremely important for all aspects of our wellbeing both at the level of our body and our brain. In recent years there has been much interest and better understanding of the role of the bacteria, viruses and other microorganisms that live in the human gut (the gut microbiome). We know that disturbing the balance between the different species of bacteria in the gut can have consequences including diarrhoea, inflammatory and autoimmune conditions and has also been linked to obesity.

There are big differences in the gut microbiome composition seen in people with untreated HIV infection compared with non-infected individuals. This disrupted balance does not seem to be restored when starting on antiretroviral therapy. Different classes of antiretrovirals seem to have different effects but this has been hard to establish because studies aiming to look at this has been large population studies where it can be hard to tease out cause and effect.

In this study we are instead aiming to compare an individual with themselves by comparing the bacterial gut microbiome before the person switches from one class of antiretroviral treatment to another or switches the delivery method of that drug, with the bacterial gut microbiome two months after the switch.

We hope that if we can understand the effects different classes and delivery methods of antiretroviral have on an individual's gut microbiome, we can take this into account when deciding on the best HIV therapy for a person. In the long term, this would lessen the negative effects of being on a life-long treatment.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    15 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    A Prospective Observational Study of the Impact on the Gut Microbiome in HIV-infected Individuals in Manchester, UK, When Switching From One Class of Antiretroviral Drugs or Delivery Method to Another Class or Delivery Method.
    Anticipated Study Start Date :
    Jan 1, 2024
    Anticipated Primary Completion Date :
    Sep 1, 2024
    Anticipated Study Completion Date :
    Dec 1, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    ART switch group

    These are individuals who complete a planned switch of ART regimen from one class of drugs or delivery method to another.

    Control group

    This group continue on their stable ART regimen.

    Outcome Measures

    Primary Outcome Measures

    1. To measure changes in diversity and abundance of bacterial species in stool sample collected before and after a change of ART. [4-8 weeks]

    Secondary Outcome Measures

    1. To link level of bacterial diversity with different ART regiments. [4-8 weeks]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Aged ≥18 years.

    • Willing to undergo stool sample collection on two occasions.

    • Able to give written, informed consent.

    • Have evidence of HIV infection

    • Have been on stable antiretroviral treatment for the previous ≥12months.

    • Planning to switch ART regimen from one class of drugs or delivery method to another.

    Exclusion Criteria:
    • HIV viral load >50 copies/ml blood

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Manchester

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gabriella Lindergard, Dr, University of Manchester
    ClinicalTrials.gov Identifier:
    NCT06100211
    Other Study ID Numbers:
    • 333914
    First Posted:
    Oct 25, 2023
    Last Update Posted:
    Oct 25, 2023
    Last Verified:
    Oct 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Gabriella Lindergard, Dr, University of Manchester
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 25, 2023