Clinical Evaluation of T.R.U.E. Test Allergens in Children an Adolescents

Status Completed

Clinical Trial Summary

The objective of the study was to evaluate the diagnostic performance and safety of T.R.U.E. Test allergens in pediatric subjects aged 6-17 years old. In total, 11 allergens were evaluated; 7 new allergens on panels 2.2 and 3.2 and 4 previously approved allergens for which changes were made to dose and excipient.

Clinical Trial Description

The evaluation of 7 new allergens on panels 2.2 and 3.2, Gold sodium thiosulfate, Hydrocortisone-17-butyrate, Bacitracin, Parthenolide, Methyldibromoglutaronitrile, Disperse blue 106, and Bronopol was the original objective of the study. The protocol was amended to include evaluation of 4 reformulated allergens; neomycin sulfate, potassium dichromate, ethylenediamne dihydrochloride and fragrance mix. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01797562
Study type	Interventional
Source	Allerderm
Contact
Status	Completed
Phase	N/A
Start date	December 10, 2012
Completion date	September 8, 2015

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