Condition 1: Diastolic dysfunction. Condition 2: Obesity. Condition 3: pre-diabetic. Left ventricular failure Overweight and obesity
Conditions
Interventions
Intervention 1: The intervention group will be treated with Empagliflozin 10 mg of Actover pharmaceutical company daily for 3 months. Cardiac function will be measured by Philips echocardiography devi
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: age more than 18 years old prediabetic (100<FBS<125) BMI more than 30 kg/m2 stability in cardiac symptom in the last 3 months
Exclusion criteria
Exclusion criteria: Using empagliflozin during the last 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The effect of empagliflozin in improving the E/e ratio after 3 months treatment. Timepoint: E/e dosing before the start of the study and after 3 months of continuous drug use. Method of measurement: Echocardiography.;FBS. Timepoint: Before the intervention and 3 months after taking Empagliflozin. Method of measurement: Blood test.;The effect of Empagliflozin on blood pressure. Timepoint: Blood pressure measurement before the start of the study and after 3 months of continuous use. Method of measurement: Pressure gauge device.;The effect of empagliflozin on lowering blood sugar by measuring 2hpp. Timepoint: Blood sugar measurement using 2hpp before the intervention and 3 months after taking Empagliflozin. Method of measurement: blood test.;The effect of empagliflozin on lowering blood sugar by measuring HbA1c. Timepoint: Blood sugar measurement using HbA1C before the intervention and 3 months after taking Empagliflozin. Method of measurement: blood test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactRoxana Sadeghi
Shahid Beheshti University of Medical Sciences
Outcome results
None listed