Clinical Trials Directory

Trials / Completed

CompletedNCT01327144

Efficacy of Oral Famciclovir Versus Aciclovir Treatment in Patients With Herpes Zoster

A Prospective, Randomized, Multicenter Study of the Efficacy and Safety of Famciclovir 500 mg Comparing To Aciclovir 400mg in Patients With Herpes Zoster

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
177 (actual)
Sponsor
EMS · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Herpes Zoster is an infection that affects part of the nervous system caused by Varicella Zoster Virus. Herpes Zoster manifests as vesicular eruption in the dermatome, often associated with significant pain. There are effective oral prescription antiviral medicines available to reduce the discomfort of symptoms as famciclovir and aciclovir. This is a phase III, multicenter, randomized, parallel-group study to compare the efficacy and safety of treatment with Famciclovir (500 mg) comparing to Aciclovir (400 mg) in patients with Herpes Zoster.

Detailed description

Study Design * single blind study, prospective, parallel group, intent to treat trial * Experiment duration: 7 days * 2 visits (days 0, and 7) * Reduction of symptoms * Adverse events evaluation

Conditions

Interventions

TypeNameDescription
DRUGFamciclovirFamciclovir 500 mg- 1 tablet each 12 hours for 7 days
DRUGAciclovirAciclovir 400 mg- 02 tablets each 4 hours for 7 days

Timeline

Start date
2012-06-01
Primary completion
2017-05-01
Completion
2017-07-01
First posted
2011-04-01
Last updated
2019-04-17

Locations

5 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01327144. Inclusion in this directory is not an endorsement.