Last updated 10 days ago
Efficacy and Safety of Madalena Association in the Treatment of Type II Diabetes Mellitus
270 patients around the world
Available in Brazil
EMS
1Research sites
270Patients around the world
This study is for people with
Diabetes
Diabetes mellitus type 2
Requirements for the patient
From 18 Years
All Gender
Medical requirements
- Ability to confirm voluntary participation and agree to all trial purposes by signing and dating the informed consent forms.Participants with 18 years of age or greater.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 at least 3 months with two anti-hyperglycemic agents (dual therapy).HbA1c ≥ 7,5% and ≤ 10,5% and fasting blood glucose > 100 mg/dL at the screening visit.BMI (body mass index) > 19 Kg/m2 and ≤ 45 Kg/m2.
- 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.Impaired renal function and end-stage renal disease.Participants with current treatment and continued for more than 15 days with systemic steroids at the time of informed consent.Impaired hepatic function.Medical history of pancreatic diseases that may suggest insulin deficiency.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.Medical history of acute coronary syndrome, stroke, unstable congestive heart failure, or respiratory failure within 6 months prior to informed consent.Current medical history of cancer and/or cancer treatment in the last 5 years.Medical history of metabolic acidosis and/or using drugs that may cause lactic acidosis.Medical history of blood dyscrasia or any other hemolytic disorders.Participants using sulfonylureas and/or insulin therapy.Treatment with anti-obesity drugs for less than 2 months or with dose change in the last 2 months.
Sites
EMS - Pharma Farmacêutica
Recruiting
SponsorEMS
Study typeInterventional
Conditions
Diabetes mellitus type 2
Requirements
From 18 YearsAll Gender
Unique study IDclinicaltrials.gov
NCT04670666
