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Clinical Trial Summary

Eligible patients will be prescribed Desloratadine 1 tablet of 5 mg once daily. Patients will be asked to follow-up for a final visit after 14 days (Day 15) where the safety, tolerability and clinical efficacy will be measured.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00724698
Study type Observational
Source Organon and Co
Contact
Status Completed
Phase
Start date October 2005
Completion date December 2007

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