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Study on the Functional Characteristics of Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes and Their Therapeutic Effects on Chronic Kidney Disease

Study on the Functional Characteristics of Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes and Their Therapeutic Effects on Chronic Kidney Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109228
Enrollment
Unknown
Registered
2025-09-15
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

Chronic kidney disease

Interventions

Stem Cell Exosomes Treatment Group 1:receive treatment with 1×10^10 particles of exosomes via intravenous infusion
Stem Cell Exosomes Treatment Group 2:receive treatment with 2×10^10 particles of exosomes via intravenous infusion
Conventional treatment group:receive medications for conventional treatment of chronic kidney disease

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Include hospitalized patients with CKD stage 2-4, specifically those with 15 < GFR <= 60 ml/min/1.73 m^2, from the Affiliated Hospital of Xuzhou Medical University between July 2025 and July 2027; 2. Conduct tests on all included patients for kidney function and other laboratory indicators, as well as kidney biopsies for those without obvious kidney atrophy; 3. Require that included patients avoid reversible factors that may promote kidney function deterioration before the study, such as hypovolemia, acute stress states, and poor blood pressure control; 4. All patients had not undergone hemodialysis or peritoneal dialysis treatment prior to the study.

Exclusion criteria

Exclusion criteria: 1. Poor blood sugar control; 2. Complicated by severe metabolic acidosis, electrolyte disorders, severe cardiovascular and cerebrovascular diseases, severe acute pancreatitis, shock, dehydration, undergoing surgical treatment, and those with indications for emergency dialysis; 3. Patients with hyperthyroidism or those taking corticosteroids; 4. Complicated by malignant tumors, respiratory diseases affecting oxygen levels, cardiovascular diseases, hematological diseases, or other severe systemic diseases; 5. Individuals who may undergo kidney transplantation during the study period; 6. Expected survival time < 12 months; 7. Pregnant or breastfeeding women; 8. Patients who participated in other drug clinical trials within 3 months prior to enrollment;9. Patients who cannot cooperate due to poor mental status or who are assessed as ineligible by clinicians for other reasons.

Design outcomes

Primary

MeasureTime frame
Renal function indicators of CKD patients after treatment with hUC-MSCs-exo;

Secondary

MeasureTime frame
Patients' kidney biopsies showed the degree of renal pathological damage after treatment with hUC-MSCs-exo.;Renal blood perfusion;

Countries

China

Contacts

Public ContactSun Dong

The Affiliated Hospital of Xuzhou Medical University

sundong126@yahoo.com+86 516 8580 6259

Outcome results

None listed

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