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NCT02706717 · ClinicalTrials.gov registry record · Phase 2

Effects of the Probiotic Visbiome Extra Strength on Gut Microbiome & Immune Activation Markers

A Phase 2 study, sponsored by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections.

Completed
Registry status
Phase 2
Development phase
93
Enrollment target

NCT02706717 is a Phase 2 study that has completed, run by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections. The registered enrollment target is 93 participants.

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The verdict

NCT02706717, a Phase 2 study, has completed, sponsored by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections.

COMPLETED
Registry status
Phase 2
Development phase
93 participants
Enrollment target

Study Summary

The purpose of the study was to evaluate whether the probiotic Visbiome Extra Strength reduces inflammation in HIV-infected men and women when compared to a placebo (inactive medication like a dummy pill). The study evaluated whether taking Visbiome Extra Strength by mouth for 24 weeks was safe and well-tolerated for HIV-infected persons on antiretroviral therapy (ART). Probiotics are germs such as yeast or bacteria that are found in food and supplements that are used to improve the health of the digestive system. Many people refer to probiotics as "helpful bacteria." These bacteria live in the body and help the body work normally. In some medical conditions, including HIV infection, helpful bacteria are replaced with bacteria that can change the normal intestinal function and increase inflammation. The investigators tested whether giving a probiotic restored normal intestinal function and decreased inflammation.

Interventions

  • DRUG Placebo
  • DRUG Visbiome Extra Strength

Trial Details

FieldValue
Enrollment Target 93 participants
Start Date 2016-04
Est. Completion 2017-08-28
Phase Phase 2

What the Registry Record Tells You About NCT02706717

The ClinicalTrials.gov registry entry for NCT02706717 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 93 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections, which has 45 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02706717 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02706717 about?

NCT02706717 is a clinical study titled "Effects of the Probiotic Visbiome Extra Strength on Gut Microbiome & Immune Activation Markers". The purpose of the study was to evaluate whether the probiotic Visbiome Extra Strength reduces inflammation in HIV-infected men and women when compared to a placebo (inactive medication like a dummy pill). The study evaluated whether taking Visbiome Extra Strength by mouth for 24 weeks was safe and ...

What is the current status of trial NCT02706717?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 93 participants. The study started on 2016-04. Estimated completion is 2017-08-28.

What interventions are being tested in trial NCT02706717?

The interventions under investigation include: Placebo (DRUG), Visbiome Extra Strength (DRUG).

Who is sponsoring clinical trial NCT02706717?

This trial is sponsored by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections, which has 45 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.