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The Impact of the Time of Drug Administration on the Effectiveness of Combined Treatment of Hypercholesterolemia With ROSuvastatin and EZEtimibe (ROSEZE) - A Single-center, Crossover, Open-label Study
The aim of the study is to demonstrate, whether the time of day of administration of the study drug (containing rosuvastatin and ezetimibe) has an impact on the effectiveness of lipid-lowering therapy.
Details
| Lead sponsor | Collegium Medicum w Bydgoszczy |
|---|---|
| Phase | Phase 4 |
| Status | COMPLETED |
| Enrolment | 83 |
| Start date | 2016-03 |
| Completion | 2020-05 |
Conditions
- Hypercholesterolemia
Interventions
- Rosuvastatin and Ezetimibe morning or evening administration
Primary outcomes
- Change in total cholesterol and LDL-Cholesterol — 6 and 12 weeks
Change in total cholesterol and LDL-Cholesterol at 6 and 12 weeks of study drug treatment (combination of ezetimibe and rosuvastatin), depending on the time of day of study drug administration
Countries
Poland