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Clinical Trial Summary

To observe the effiacay, safety and risk of developing diabetes, review the patients chars who had administrated or neet to administrate the Pravafenix cap for enroll period, it is an prospective observational study that only collect the collectable information follwoing the hospital visiting date from enroll point to information collecting date. There is no extra visit for this study.

Observe the data which has been collected for 3 yearts every year from enroll point, if the patients agree to be participated in this study and are suitable in inclusion/exclusion criteria.

If the lipid-lowering drugs(only Ezetimibe is possible) is add-on the Pravafenix Cap administrating period, it will be analyzed by laering analysis separately. But, the reason why it is add-on to have to be written on e-CRF.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03214211
Study type Observational
Source Yooyoung Pharmaceutical Co.,Ltd.
Contact Min-Kyung Kwon, Manager
Phone 82-2-6202-7104
Email mkkwon@yypharm.co.kr
Status Not yet recruiting
Phase N/A
Start date August 30, 2017
Completion date June 30, 2022

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