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Assessment of the Efficacy and Tolerability of the Fixed-dose Combination of Bisoprolol/Perindopril — STYLE  

Arterial Hypertension Clinical Trial

Official title:
Multicenter Observational Open Program. Assessment of the Efficacy and Tolerability of the Fixed-dose Combination of Bisoprolol/Perindopril in Patients With Arterial Hypertension and Stable CAD in Daily Clinical Practice (STYLE)

Clinical Trial Summary

Study objective - to assess the efficacy, tolerability and adherence of bisoprolol/perindopril FDC in patients with HT and stable CAD in everyday practice. Type of the program: multicenter, observational, uncontrolled, open program. The program will involve 480 general practitioners (GPs) and cardiologists from the primary care facilities.Each doctor includes four patients. It is planned to include not less than 1920 patients in total.

Clinical Trial Description

Multicenter observational open program. Assessment of the efficacy and tolerability of the fixed-dose combination of bisoprolol/perindopril in patients with arterial hypertension and stable CAD in daily clinical practice (STYLE) Study objectives and purposes: Primary endpoints: - efficacy of bisoprolol/perindopril FDC in patients with HT and stable CAD in everyday practice regarding the BP - efficacy of bisoprolol/perindopril FDC in patients with HT and stable CAD in everyday practice regarding the angina Secondary endpoints: - impact on the quality of life of bisoprolol/perindopril FDC in patients with HT and stable CAD in everyday practice - adherence to bisoprolol/perindopril FDC therapy in patients with HT and stable CAD in everyday practice The program will involve 480 general practitioners (GPs) and cardiologists from the primary care facilities. Each doctor includes four patients. It is planned to include not less than 1920 patients in total. Milestones of the program: FSI - November, 2018 LSLV- January, 2019 Database Lock - February, 2019 Statistic Report- May, 2019 Clinical Study Report- January, 2020 ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03730116
Study type Observational
Source Servier Russia
Contact
Status Completed
Phase
Start date November 14, 2018
Completion date October 24, 2019
View Details
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