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Evaluation of remission effect in patients with type 2 diabetes induced by the combination of metformin, SGLT2i and GLP-1RA

Evaluation of remission effect in patients with type 2 diabetes induced by the combination of metformin, SGLT2i and GLP-1RA

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091159
Enrollment
Unknown
Registered
2024-10-22
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

Type 2 Diabetes Mellitus

Interventions

Trail group:None

Sponsors

Dongying People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged at least 18 years of age; 2. A diagnosis of type 2 diabetes and course within 5 years; 3.GADA and other type 1 diabetes-related antibodies are negative; 4. Fasting blood glucose between 7.0-11.0mmol/L, HbA1c above 7.0%, fasting C-peptide =1.1µg/L, BMI>25kg/m2; 5. Combination of metformin, SGLT2i(dapagliflozin/empagliflozin/constagliflozin/itogagliflozin/canagliflozin) and GLP-1RA(loseenatide/semaglutide/duraglutide/liraglutide) was newly used in the past 3 months and currently used regularly to control blood glucose; 6. Are receiving diabetes related lifestyle guidance; 7. Willing to participate in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. With type 1 diabetes, gestational diabetes, or other special types of diabetes; 2. There are serious heart, liver, kidney, nerve, blood or endocrine system diseases; 3. There are serious infection, trauma, surgery, or other irritability disease; 4. Severe gastrointestinal disease or malabsorption syndrome; 5. Severe mental illness or cognitive impairment; 6. A history of acute pancreatitis, urinary tract or genital infection; 7. Any kind of drugs in the 221 plan the composition of the allergy or intolerance. 8. Use of other glucose-lowering medications or participation in other clinical trials within the past 3 months.

Design outcomes

Primary

MeasureTime frame
glycated hemoglobin;

Secondary

MeasureTime frame
blood biochemical indicators;liver function;blood lipid profile;insulin;C-peptide;routine urine test;urinary albumin;body mass index;Chinese Visceral Adiposity Index(CVAI);Fatty liver degree;Muscle content;

Countries

China

Contacts

Public ContactXu Chao

Dongying People's Hospital

doctorxuchao@163.com+86 156 2884 1616

Outcome results

None listed

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