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Clinical Trial Summary

The aim of this observational study is to document the therapeutic use of PASCALLERG ® for hay fever. Based on the survey is a decrease in disease-specific symptoms when taking PASCALLERG ® over a period of 4 weeks will be documented. In addition to the compatibility can be assessed.


Clinical Trial Description

There are documented male and female patients over the age of one year who suffer from hay fever. The traetment time is about a period of 4 weeks with PASCALLERG® tablets. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01660737
Study type Observational
Source Pascoe Pharmazeutische Praeparate GmbH
Contact
Status Completed
Phase
Start date February 2012
Completion date July 2013

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