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An Exploratory Clinical Trial of Ursodeoxycholic Acid for Early Diabetic Kidney Disease

An Exploratory Clinical Trial of Ursodeoxycholic Acid for Early Diabetic Kidney Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128420
Enrollment
Unknown
Registered
2026-07-20
Start date
2026-07-21
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Early-stage diabetic kidney disease

Interventions

Intervention group:Ursodeoxycholic acid Tablets (Pyrifos) (250mg*24 tablets per box) : 10mg/kg, 2-3 tablets per day, oral. The treatment course is 8 weeks.

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years, both genders. 2. eGFR >=60 ml·min^-1·(1.73 m^2)^-1, and UACR 30-300 mg/g (i.e., G1A2, G2A2). 3. HbA1C <=8.5%. 4. Blood pressure <=130/80 mmHg. 5. The subject (or their legally authorized representative) has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those with severe primary diseases of the heart, brain, liver and hematopoietic system, etc. 2. Those who have experienced acute metabolic disorders such as diabetic ketoacidosis within the past month; 3. Those with positive HBV serological indicators other than HbsAb and those with abnormal transaminase levels in continuous liver function tests; 4. Participated in other clinical studies within two months prior to the start of the research; 5. Pregnant or lactating women; 6. Patients with confusion, dementia, various mental illnesses and those who are unwilling to cooperate.

Design outcomes

Primary

MeasureTime frame
Urinary microalbumin/urinary creatinine;Renal function (Scr, eGFR);Glycated hemoglobin (HbA1C);

Secondary

MeasureTime frame
Cholesterol (TC), triglycerides (TG), high-density lipoprotein (HDL), low-density lipoprotein (LDL).;Adverse event;Vital signs: body temperature, resting heart rate, blood pressure, etc;Demographic characteristics: gender, age, height, weight;

Countries

China

Contacts

Public ContactLi Ting

The First Affiliated Hospital of Xi'an Jiaotong University

tingli1@xjtu.edu.cn+86 29 85323810

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026