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NCT00723229 · ClinicalTrials.gov registry record · Phase 4

A Randomized Trial to Evaluated the Suppressive Effect of Acyclovir on Rapidly Cleared HSV-2 Reactivation

A Phase 4 study, sponsored by University of Washington.

Completed
Registry status
Phase 4
Development phase
48
Enrollment target

NCT00723229 is a Phase 4 study that has completed, run by University of Washington. The registered enrollment target is 48 participants.

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The verdict

NCT00723229, a Phase 4 study, has completed, sponsored by University of Washington.

COMPLETED
Registry status
Phase 4
Development phase
48 participants
Enrollment target

Study Summary

We propose to study the episode rate, duration, and quantity of HSV-2 genital shedding in patients taking standard, FDA approved, CDC recommended doses of acyclovir (400 mg PO BID) for HSV-2 suppression compared to taking no medication to better define the effect of acyclovir on short bursts of rapidly cleared HSV-2 shedding. This study will be a randomized, open label, cross-over trial. We hypothesize that short bursts of HSV-2 reactivation will not be suppressed by acyclovir.

Interventions

  • DRUG acyclovir

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2008-08
Est. Completion 2011-09
Phase Phase 4

Sponsor

University of Washington

1,048 total trials

What the Registry Record Tells You About NCT00723229

The ClinicalTrials.gov registry entry for NCT00723229 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.

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

NCT00723229 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00723229 about?

NCT00723229 is a clinical study titled "A Randomized Trial to Evaluated the Suppressive Effect of Acyclovir on Rapidly Cleared HSV-2 Reactivation". We propose to study the episode rate, duration, and quantity of HSV-2 genital shedding in patients taking standard, FDA approved, CDC recommended doses of acyclovir (400 mg PO BID) for HSV-2 suppression compared to taking no medication to better define the effect of acyclovir on short bursts of rapi...

What is the current status of trial NCT00723229?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 48 participants. The study started on 2008-08. Estimated completion is 2011-09.

What interventions are being tested in trial NCT00723229?

The interventions under investigation include: acyclovir (DRUG).

Who is sponsoring clinical trial NCT00723229?

This trial is sponsored by University of Washington, which has 1,048 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.