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Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of quetiapine in actual clinical settings.


Clinical Trial Description

This is a post-marketing use-result survey study required for products in Japan. The investigator will register the patient who have been taking this product for the first time within 14 days after the start of treatment (inclusive of the start day). For each of the registered patients (including withdrawals and dropouts), the investigator will enter the survey data on the case report form. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03403790
Study type Observational
Source Astellas Pharma Inc
Contact
Status Completed
Phase
Start date January 15, 2018
Completion date March 19, 2020

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