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Clinical Trial Summary

The purpose of this study is to compare the safety and efficacy of Vacyless® and Valtrex® in patients with acute herpes zoster.


Clinical Trial Description

Primary Endpoint:

- Lesion assessment - Rash severity, in terms of rash counts

Secondary Endpoints:

- Pain assessment

- Clinical global impression

- Safety information of valacyclovir ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02152800
Study type Interventional
Source Yung Shin Pharm. Ind. Co., Ltd.
Contact
Status Completed
Phase Phase 4
Start date April 2011
Completion date November 2013

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