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Efficacy and Safety Analysis of Combined Therapy with Glargine Insulin, Liraglutide, and Metformin in Type 2 Diabetes

Efficacy and Safety Analysis of Combined Therapy with Glargine Insulin, Liraglutide, and Metformin in Type 2 Diabetes

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084794
Enrollment
Unknown
Registered
2024-05-24
Start date
2022-11-04
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes

Interventions

Treatment group:After 7-10 days of intensive insulin pump treatment, the combination of insulin glargine, metformin hydrochloride and liraglutide was given
Control group:After 7-10 days of intensive insulin pump therapy, metformin hydrochloride, daglipzin and acarbose were given combined therapy

Sponsors

Guangrao County People's Hospital of Dongying city
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Screening patients diagnosed with type 2 diabetes mellitus (clinical diagnosis) and disease duration =5 years; (2) Poor blood glucose control (HbA1c=7.5% and =10.5%), FPG>7.5mmol/L or 2hFBG>10mmol/L; (3) Maintaining the current stable regimen for at least =3 months (treatment with 2-3 oral hypoglycemic drugs, such as metformin, sulfonylurea, STZ, glienides, a-glucosidase inhibitors, DPP-4i, SGLT-2i, etc.); (4) Age =18 years, BMI=20kg/m2.

Exclusion criteria

Exclusion criteria: (1) GLP-1RA and various types of insulin have been used in the last 3 months; (2) Have participated in other scientific research or clinical trial projects within the past 4 weeks; (3) DKA or NKHS has ever occurred; (4) Have a history of major cardiovascular disease: acute or chronic myocardial infarction, unstable angina pectoris or malignant arrhythmia, acute or chronic heart failure (NYHA grade ?, ?), and have a history of major cardiac or interventional vascular surgery; (5) Rapid progression of kidney disease or other types of kidney disease that have not yet been diagnosed; (6) Active liver disease or liver insufficiency (AST or ALT greater than 2 times the upper limit of normal); (7) Proliferative retinopathy (fundus hemorrhage); (8) is currently pregnant or breastfeeding; (9) A long history of uncontrolled alcoholism or drug abuse; (10) History of unstable mental illness.

Design outcomes

Primary

MeasureTime frame
Fasting Blood Glucose;Glycated Hemoglobin ;Fasting C-peptide;

Secondary

MeasureTime frame
Glycated albumin;Full fasting insulin;Triglycerides;Total cholesterol;Low-density lipoprotein cholestero;serum creatinine;cystatin C;24-hour urinary protein quantity;hypersensitive reactive protein;

Countries

China

Contacts

Public ContactGao Yuan

Department of Endocrinology, Guangrao County People's Hospital of Dongying city

81248103@qq.com+86 131 8196 1861

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026