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The clinical study of mesenchymal stem cells in the treatment of early diabetic nephropathy

The clinical study of mesenchymal stem cells in the treatment of early diabetic nephropathy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056539
Enrollment
Unknown
Registered
2022-02-07
Start date
2022-03-01
Completion date
Unknown
Last updated
2024-10-07

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

Conditions

Diabetic nephropathy (DN)

Interventions

Experimental group:Mesenchymal stem cell intravenous injection+standardized treatment measures
Control group:Standard treatment

Sponsors

The Second Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients with early diabetic nephropathy were selected according to the World Health Organization (WHO) diagnostic criteria for type 2 diabetes in 1999 and Mogensen and other DN staging criteria; 2. Gender is unlimited, aged 30-65 years; 3. Urine albumin excretion rate (UAER) of at least 2 consecutive times within 6 months is 20-200 µg/min (30-300 mg/24h), glomerular filtration rate (GFR) 70-30 mL/min, or continuous urine protein<0.5 g/24h, serum creatinine (SCR) and creatinine clearance rate (CCr) were within normal range; 4. The patient has received renal biopsy within 6 months, and the pathological diagnosis is consistent with DN, or although no renal biopsy is performed, the clinical diagnosis is consistent with DN; 5. The patient has good compliance and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Participated in other clinical trials within 30 days before the start of this study; 2. Pregnant or lactating patients; 3. Plasma albumin (ALB)= 160mmHg or diastolic blood pressure >= 100mmHg) and it is difficult to control; 7. Complicated with urinary tract infection, ketoacidosis, heart failure (heart failure), pulmonary infection and tumor; 8. Use of nephrotoxic drugs; 9. Have a history of mental illness or other incompatibility factors.

Design outcomes

Primary

MeasureTime frame
albumin;24 hours urine protein quantification;

Secondary

MeasureTime frame
blood sugar;

Countries

China

Contacts

Public ContactLiu Gang

The Second Hospital of Shandong University

lg-2000@163.com+86 17660086617

Outcome results

None listed

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