Study on the Efficacy aNd Safety of Jinlida Granules in Patients With Inadequately cOntrolled tYpe-2 Diabetes and dysLIpidemia Under liFe Style Intervention (ENJOY LIFE Study)
Phase 4
- Conditions
- Type 2 DiabetesDyslipidemia
- Interventions
- Drug: placebo granules
- Registration Number
- NCT02035644
- Lead Sponsor
- Shanghai Jiao Tong University School of Medicine
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 360
Inclusion Criteria
- age of 20-70 years;
- diagnosed with type 2 diabetes inadequately controlled under life style intervention with 3 months before screening;
- HbA1c ≥6.5% and ≤10.0%, and fasting plasma glucose ≥7 and ≤13.3mmol/L at baseline;
- diagnosed with dislipidemia with triglycerides>150mg/dL (1.70mmol/L), and/or total cholesterol >200mg/dL (5.16mmol/L), and/or LDL-c>100mg/dL (2.58mmol/L)
- body mass index (BMI): 20<BMI<40 kg/m2;
Exclusion Criteria
- moderate or severe liver dysfunction, abnormal renal function;
- severe dysfunction of the heart;
- histories of acute diabetic complications including diabetic ketoacidosis or hyperosmolar hyperglycemic non-ketotic coma within 3 months;
- psychiatric disease or severe infection;
- pregnancy or planned pregnancy;
- use of any drug (including insulin) for treatment of diabetes or dyslipidemia within 3 months;
- use of chronic (>7 days) systemic glucocorticoid therapy within 8 weeks or receive growth hormone therapy within 6 months;
- diagnosed with type 1 diabetes, or gestational diabetes, or other specific types of diabetes;
- history of malignant tumor within 5 years.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Jinlida granules Jinlida granules Jinlida granules, a traditional Chinese medicine, was a herbal formula which was developed under cognition of the theory in the onset of diabetes placebo granules placebo granules placebo prepared in indistinguishable granules
- Primary Outcome Measures
Name Time Method change in HbA1c levels 16 weeks
- Secondary Outcome Measures
Name Time Method BMI 16 weeks blood pressures 16 weeks fasting, postload 30-min and 2-h plasma glucose 16 weeks fasting, postload 30-min and 2-h serum insulin 16 weeks serum lipids 16 weeks glucose disposal rate (GDR) values from hyperinsulinemic euglycemic clamp 16 weeks incretins 16 weeks metabolomic parameters 16 weeks
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie Jinlida granules' effects on insulin resistance and lipid metabolism in type 2 diabetes and dyslipidemia?
How does Jinlida granules' efficacy compare to standard-of-care antidiabetic and lipid-lowering therapies in phase 4 trials?
Which biomarkers could predict patient response to Jinlida granules in combination with lifestyle interventions for metabolic syndrome?
What are the potential adverse events associated with Jinlida granules in long-term management of hyperglycemia and dyslipidemia?
How do Jinlida granules interact with other antidiabetic agents like SGLT2 inhibitors or GLP-1 receptor agonists in combination therapy?
Trial Locations
- Locations (1)
Guang Ning
🇨🇳Shanghai, Shanghai, China
Guang Ning🇨🇳Shanghai, Shanghai, China