The aim of the present study is to evaluate the efficacy and safety of Jinlida granules in patients with inadequately controlled type-2 diabetes and dyslipidemia under life style intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
360
Guang Ning
Shanghai, Shanghai Municipality, China
change in HbA1c levels
Time frame: 16 weeks
fasting, postload 30-min and 2-h plasma glucose
Time frame: 16 weeks
fasting, postload 30-min and 2-h serum insulin
Time frame: 16 weeks
serum lipids
Time frame: 16 weeks
glucose disposal rate (GDR) values from hyperinsulinemic euglycemic clamp
Time frame: 16 weeks
incretins
Time frame: 16 weeks
metabolomic parameters
Time frame: 16 weeks
BMI
Time frame: 16 weeks
blood pressures
Time frame: 16 weeks
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