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UnknownNCT03214211

Prospective Observational Study of Pravafenix Cap

Assess the Long-term Safety and Efficacy of Pravafenix Cap. in Korean Patients With Dyslipidemia: a Multicenter, Prospective, Observational Study

Status
Unknown
Phase
Study type
Observational
Enrollment
3,088 (estimated)
Sponsor
Yooyoung Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2017-08-30
Primary completion
2022-06-30
Completion
2022-06-30
First posted
2017-07-11
Last updated
2017-08-31

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03214211. Inclusion in this directory is not an endorsement.

Prospective Observational Study of Pravafenix Cap (NCT03214211) · Clinical Trials Directory