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Clinical Trial Summary

Patients enrolled into the study will be randomly allocated either to Empagliflozin group or control group. In the Empagliflozin group patients will be receiving standard care + Empagliflozin 10 mg o.d., in the control group patients will be receiving standard care without sodium glucose contransporter 2 (SGLT2) inhibitors.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03753087
Study type Interventional
Source National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
Contact Fail Ageev, MD, PhD
Phone +74954146612
Email ftageev@gmail.com
Status Recruiting
Phase Phase 4
Start date January 16, 2019
Completion date May 2020

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