This is a prospective, randomized, open-label, active drug controlled clinical trial that aims to compare the effects of henagliflozin or metformin on myocardial tissue level characteristics in type 2 diabetes patients with obesity. Eligible subjects with type 2 diabetes before randomisation and fulfilling all of the inclusion criteria and none of the exclusion criteria will be randomised in a 1:1 ratio to henagliflozin 10 mg once a day or metformin 1000 mg twice a day and treated for 24 weeks. The study includes five visits.
MRI scanning will be assessed at baseline and at the end of the treatment period in order to to assess the cardiac morphology, cardiac function, and myocardial tissue characteristics. The cardiac MRI examination will be performed in accordance with a pre-defined MRI protocol. Images from all sites will be analyzed centrally at the core-lab using a dedicated software package and certified analysts.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
64
Henagliflozin 10mg qd po
Metformin 1000mg bid po
Extra-cellular volume fraction
To compare the effects of henagliflozin and metformin on extra-cellular volume fraction
Time frame: baseline and week 24
Mean Change in HbA1c Levels
To compare the effects of henagliflozin and metformin on HbA1c Levels
Time frame: baseline and week 24
Mean change in body mass index
To compare the effects of henagliflozin and metformin on body mass index
Time frame: baseline and week 24
Mean change in blood pressure
To compare the effects of henagliflozin and metformin on blood pressure
Time frame: baseline and week 24
Mean change in level of Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)
To compare the effects of henagliflozin and metformin on level of Homeostatic Model Assessment of Insulin Resistance
Time frame: baseline and week 24
Native T2 mapping
To compare the effects of henagliflozin and metformin on native T2 mapping
Time frame: baseline and week 24
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