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Clinical Trial Summary

The study is designed as a randomized, double-blind, parallel-group, multi centre study comparing perception and tolerability of investigational product and comparator. In the randomized part of the study the subjects will be given either LoFric Primo (POBE) or the comparator LoFric Primo (PVC) for use over 4 weeks. The hypothesis is that subject perception and satisfaction of POBE is equal to or better than for PVC.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00753298
Study type Interventional
Source Wellspect HealthCare
Contact
Status Completed
Phase N/A
Start date January 2007
Completion date March 2008

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