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Clinical Trial Summary

Several studies have been done on the efficacy of the herbal medicine Iberogast. In this study researcher want to learn more about the time needed for Iberogast to start to work after the patient took the drug. This study plans to enroll 300 adult male and female patients suffering from disturbance of stomach and intestine normal function and treated by their doctor with Iberogast drops. Patients will be asked to document on a diary card the changes of symptom severity of the stomach and intestine complaints and the time needed for the symptoms to improve after drug intake. At the end of the study the treating doctor and the patients will be asked about the overall changes of symptoms. In addition information on the safety of the drug and how well the drug is tolerated by the patients will be collected


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04059783
Study type Observational
Source Bayer
Contact
Status Completed
Phase
Start date June 17, 2008
Completion date February 20, 2011

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