Dyslipidemia Associated With Type II Diabetes Mellitus
Conditions
Keywords
Dyslipidemia, Type II Diabetes Mellitus
Brief summary
The purpose of this study is to evaluate the efficacy and safety of Berlim 25/20 association in the treatment of type 2 diabetes mellitus and dyslipidemia.
Interventions
DRUGBERLIM 25/20 ASSOCIATION
Berlim 25/20 association coated tablet.
Empagliflozin placebo coated tablet.
Rosuvastatin calcium placebo coated tablet.
DRUGEMPAGLIFLOZIN
Empagliflozin 25 mg coated tablet.
Rosuvastatin 20 mg coated tablet.
OTHERBERLIM 25/20 ASSOCIATION PLACEBO
Berlim 25/20 association placebo coated tablet.
Sponsors
EMS
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Ability to confirm voluntary participation and agree to all trial purposes by signing and dating the informed consent forms; * Participants of both sexes, with age greater than or equal to 18 years and less than or equal to 85 years; * Participants presenting the diagnosis of type II diabetes mellitus, and who did not reach the therapeutic goals of HbA1c with previous dietary, physical exercise guidance and previous therapies at a stable dose in the last 3 months; * HbA1c ≥ 7,5% and ≤ 10,5% and fasting blood glucose \> 100 mg/dL at the screening visit; * Participants with high or very high cardiovascular risk according to the Brazilian guideline on the prevention of cardiovascular diseases in patients with diabetes (2017), which have not reached the goal of LDL-c ≤ 70 mg/dL or ≤ 50 mg/dL, respectively, with lifestyle changes, who are or aren't using low or moderate potency statins; * BMI (body mass index) \> 19 Kg/m2 and ≤ 45 Kg/m2.
Exclusion criteria
* Any clinical and laboratory findings that, in the judgment of the investigator, may interfere with the safety of research participants; * History of alcohol abuse or illicit drug use; * Participation in a clinical trial in the year prior to this study; * Pregnancy or risk of pregnancy and lactating patients; * Known hypersensitivity to the formula components used during the clinical trial; * Type 1 diabetes mellitus; * Fasting blood glucose \> 300 mg/dL; * Risk factors for volume depletion; * Participants with total cholesterol \> 500 mg/dL or triglycerides \> 500 mg/dL; * Impaired renal function and end-stage renal disease; * Participants with known heart failure, class III to IV (New York Heart Association); * Impaired hepatic function; * Medical history of pancreatic diseases that may suggest insulin deficiency; * Participants who had any cardiovascular event (acute myocardial infarction, acute coronary syndrome, recent onset stable angina, stroke, unstable congestive heart failure requiring treatment change), underwent revascularization or vascular surgery in the 6 months prior to screening; * Bariatric surgery in the last two years and/ or other gastrointestinal surgeries that can cause chronic malabsorption syndrome; * Condition that, in the investigator's judgment, may favor clinically significant changes in CPK levels; * Current medical history of cancer and/ or cancer treatment in the last 5 years; * Participants with known uncontrolled hypothyroidism or TSH levels \> 5 mIU/L; * History of known muscle disease or prior statin intolerance; * Participants using SGLT2 inhibitors, sulfonylureas and/or insulin therapy or PCSK9 inhibitors; * Participants who used other medications with prominent action in the control of serum triglyceride and cholesterol levels in the last 4 weeks or who are using low or moderate-intensity statins that cannot be replaced by rosuvastatin 20 mg; * Participants using medications that may interfere with triglyceride and cholesterol metabolism started less than 4 weeks ago or with dose adjustment in the last 4 weeks prior to the screening visit; * Treatment with anti-obesity drugs for less than 2 months or with dose change in the last 2 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of glycated hemoglobin levels measured between the first visit and the last visit. | 120 days |
| Percentual reduction of LDL-c levels measured between the first visit and the last visit. | 120 days |
Secondary
| Measure | Time frame |
|---|---|
| Incidence and severity of adverse events recorded during the study. | 150 days |
Countries
Brazil
Contacts
Primary ContactCassiano O Berto, BD
Outcome results
None listed