Bioequivalence of Ethylenediamine Dihydrochloride Study

Status Completed

Clinical Trial Summary

The purpose of this study is to compare the allergen ethylenediamine dihydrochloride when prepared using methylcellulose versus preparation using polyvinylpyrrolidone.

Clinical Trial Description

We propose an open, prospective, single-site study to evaluate the bioequivalence of ethylenediamine dihydrochloride in methylcellulose (MC)and polyvinylpyrrolidone (PVP) formulations. Bioequivalence will be determined in minimum of 15 adult subjects, with a clinical history of contact dermatitis and a positive patch test (current or previous) to ethylenediamine ("sensitives"). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01798589
Study type	Interventional
Source	Allerderm
Contact
Status	Completed
Phase	Phase 4
Start date	July 2012
Completion date	August 2012

View Details

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