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NCT00109603 · ClinicalTrials.gov registry record · NA

Effect of Tenofovir Disoproxil Fumarate on Lipid Levels in HIV Infected Adults on Stable Anti-HIV Drug Therapy

A NA study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
NA
Development phase
17
Enrollment target

NCT00109603 is a NA study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 17 participants.

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The verdict

NCT00109603, a NA study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
NA
Development phase
17 participants
Enrollment target

Study Summary

The purpose of this study is to determine the effect of the anti-HIV drug tenofovir disoproxil fumarate (TDF) on lipid levels in HIV infected adults on stable anti-HIV drug therapy. Study hypothesis: The addition of TDF to stable background antiretroviral therapy in HIV infected individuals with dyslipidemia will result in a reduction of non-HDL after 12 weeks of treatment.

Interventions

  • DRUG Tenofovir disoproxil fumarate

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2005-05
Est. Completion 2007-11
Phase NA

What the Registry Record Tells You About NCT00109603

The ClinicalTrials.gov registry entry for NCT00109603 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 17 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Tenofovir disoproxil fumarate is the first listed.

NCT00109603 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00109603 about?

NCT00109603 is a clinical study titled "Effect of Tenofovir Disoproxil Fumarate on Lipid Levels in HIV Infected Adults on Stable Anti-HIV Drug Therapy". The purpose of this study is to determine the effect of the anti-HIV drug tenofovir disoproxil fumarate (TDF) on lipid levels in HIV infected adults on stable anti-HIV drug therapy. Study hypothesis: The addition of TDF to stable background antiretroviral therapy in HIV infected individuals with dy...

What is the current status of trial NCT00109603?

This trial is currently completed. It is a NA study. The enrollment target is 17 participants. The study started on 2005-05. Estimated completion is 2007-11.

What interventions are being tested in trial NCT00109603?

The interventions under investigation include: Tenofovir disoproxil fumarate (DRUG).

Who is sponsoring clinical trial NCT00109603?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

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

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.