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NCT00926120 · ClinicalTrials.gov registry record · Phase 2

The Effects of Mogroside Sweetener on Viral Load in TreatmenT Naive Genotype 1 (GT 1) Subjects CHC

A Phase 2 study, sponsored by Brooke Army Medical Center.

Completed
Registry status
Phase 2
Development phase
10
Enrollment target

NCT00926120: Completed Phase 2 study, sponsored by Brooke Army Medical Center.

NCT00926120 is a Phase 2 study that has completed, run by Brooke Army Medical Center. The registered enrollment target is 10 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00926120, a Phase 2 study, has completed, sponsored by Brooke Army Medical Center.

COMPLETED
Registry status
Phase 2
Development phase
10 participants
Enrollment target

Study Summary

The purpose of this study is to determine if administering Mogroside Sweetener "PureLo" (the study substance) for 14 days will lower the hepatitis C viral load and liver function alanine aminotransferase (ALT) levels.

Interventions

  • DIETARY_SUPPLEMENT Mogroside sweetener (PureLo)

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2008-12
Est. Completion 2010-01
Phase Phase 2
Brooke Army Medical Center

54 total trials

What the finished NCT00926120 record still lists

NCT00926120 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Mogroside sweetener (PureLo) is the first listed.

NCT00926120 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00926120 about?

NCT00926120 is a clinical study titled "The Effects of Mogroside Sweetener on Viral Load in TreatmenT Naive Genotype 1 (GT 1) Subjects CHC". The purpose of this study is to determine if administering Mogroside Sweetener "PureLo" (the study substance) for 14 days will lower the hepatitis C viral load and liver function alanine aminotransferase (ALT) levels.

What is the current status of trial NCT00926120?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2008-12. Estimated completion is 2010-01.

What interventions are being tested in trial NCT00926120?

The interventions under investigation include: Mogroside sweetener (PureLo) (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT00926120?

This trial is sponsored by Brooke Army Medical Center, which has 54 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00926120's enrollment target sits among peer trials

10 1968th of 2000 higher than 12 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00926120, the US trial registry maintained by the National Library of Medicine. NCT00926120 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.