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Clinical Trial Summary

Secondary Data Collection:To confirm the safety and effectiveness profiles under the actual medical practice of Precedex in Japan.


Clinical Trial Description

To assess the data, including safety profile, of Precedex Intravenous Solution administered for "sedation during and after mechanical ventilation in the intensive care setting" in pediatric patients under actual medical practice in Japan. Maruishi Pharmaceutical Co., Ltd. and Pfizer Japan Inc. will collect 50 subjects each. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04040439
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date July 30, 2019
Completion date August 8, 2022

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