Left Ventricular Functional Changes of Uncontrolled Diabetes by Dapagliflozin Treatment Trial

The ELUCIDATE trial is a prospective, open label, randomized, active-controlled 'proof of concept'single centre study conducted in Mackay Memorial Hospital, Taipei, Taiwan. It is designed to clarify the LV remodeling by using Speckle-Tracking echocardiography to measure cardiac global longitudinal strain (GLS).

A cohort of 90 type 2 DM patients with normal LV ejection fraction will be randomized to either dapagliflozin 10 mg/die or to standard of care group as an active comparator. The study consists of 5 visits (see Table 1) and will last half an year, which has been ongoing since February 2019.

The primary outcomes are to detect the changes in LV mass index and cardiac GLS from baseline to 6 months after treatment initiation. The secondary outcomes include changes from baseline to 6 months in anthropometric measures, atrial-ventricular mechanics measurements, HbA1C,Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), epicardial fat and plasma biomarkers regarding cardiomyocyte remodeling and inflammation.

Inclusion criteria

• Male or female affected by type 2 diabetes mellitus (T2D) for at least 6 months.
• Age ≥ 20 and ≤ 80 years.
• HbA1c levels 7.1%~9.0% .
• On stable (at least 3 months) antidiabetic therapy with SGLT2 inhibitors naive.
• On stable (at least 3 months) cardio-active therapies (e.g. anti-hypertensive drugs, diuretics or drugs for hyperlipidemia).
• Preserved kidney function as defined by estimated glomerular filtration rate(eGFR)> 60 mL/min/1.73m2.
• Preserved left ventricular function defined as EF ≥ 50% by echocardiographic screening.

Exclusion criteria

Subjects should not enter the study if any of the following exclusion criteria are fulfilled:

• Involvement in the planning and/or conduct of the study (applies to both Investigator staff and/or staff at the study site).
• Previous enrolment or randomisation in the present study.
• Participation in another clinical study with an investigational product during the last 3 months.

The exclusion criteria that follow are for example only; include, exclude, modify or add other criteria as appropriate.

• Refuse or inability to give informed consent.
• Patients unlikely to comply with the protocol or unable to understand the nature and possible consequences of the study.
• Employees of the investigator or study centre (i.e. principal investigator, sub-investigator, study coordinators, other study staff, employees, or contractors of each), with direct involvement in the proposed study or other studies under the direction of that investigator and/or study centre, as well as family members of the employees or the investigator.
• Pregnancy or active breast feeding.
• History of hospitalization for heart failure.
• History of stage C or D heart failure.
• History of myocardial infarction.
• History of cardiac dysrhythmia.
• Patients with a known hypersensitivity to Dapagliflozin or any of the excipients of the product.