Fexofenadine in Pruritic Skin Disease

Status Completed

Clinical Trial Summary

Primary objective:

- To compare the efficacy and safety profile of Fexofenadine 180mg tablets plus prednicarbate(2.5mg/g) vs prednicarbate(2.5mg/g) alone in the treatment of pruritic skin disease

Secondary objective:

- To evaluate patient's satisfaction of Allegra treatment

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00261079
Study type	Interventional
Source	Handok Pharmaceuticals Co., Ltd.
Contact
Status	Completed
Phase	Phase 4
Start date	April 2005
Completion date	October 2006

View Details

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