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Study on the clinical efficacy and mechanism of constant gliflozin tablets in the treatment of microalbuminuria in type 2 diabetic nephropathy

Study on the clinical efficacy and mechanism of constant gliflozin tablets in the treatment of microalbuminuria in type 2 diabetic nephropathy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088947
Enrollment
Unknown
Registered
2024-08-29
Start date
2024-06-09
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

Type 2 diabetic nephropathy

Interventions

control group:Irbesartan tablets (Oral, 2 tablets 75mg per tablet, once per day)
treatment group :Constant Gliflozin tablets (Oral, 1 tablet/time, 10mg per tablet, once/day)

Sponsors

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria for microalbuminuria phase of type 2 diabetic nephropathy; (2) Aged 18 to 70 years old (including 18 and 70), gender is not limited; (3)7.0% <= HbA1c <= 11%; (4) The subject was informed and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with type 1 diabetes mellitus, gestational diabetes mellitus and other special types of diabetes mellitus; (2) Kidney damage caused by non-diabetic nephropathy; (3) Blood pressure >=160 / 100mmHg; (4) Patients with acute complications of diabetes mellitus; (5) Severe cardiac and cerebrovascular diseases and serious primary diseases, such as liver, kidney and hematopoietic system; (6) People with known allergies and allergic constitution to the study drug; (7) Pregnant and lactating women and women with recent family planning; (8) Long-term alcoholism, drug dependence, and patients with mental illness; (9) Those who have participated in or are participating in other drug clinical trials within one month before the screening period of the study; (10) The glomerular filtration rate is <45 ml min^(-1)*(1.73 m²)^(-1); (11) The investigator is not inappropriate to attend the clinical investigator.

Design outcomes

Primary

MeasureTime frame
Urinary albumin / creatinine;

Secondary

MeasureTime frame
fasting blood-glucose;glycosylated hemoglobin ;Blood glucose was obtained 2h after meal;G. F. R. ;

Countries

China

Contacts

Public ContactZhao Jindong

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine

zhaojindong1111@163.com+86 152 5657 1336

Outcome results

None listed

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