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The clinical research on the protective effects of erythropoietin in ischemia-reperfusion injury of the transplanted kidney

The clinical research on the protective effects of erythropoietin in ischemia-reperfusion injury of the transplanted kidney

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057645
Enrollment
Unknown
Registered
2022-03-15
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

the ischemia-reperfusion injury of the transplanted kidney

Interventions

Experimental group:Intravenous injection of EPO (300 IU/kg)
Control group:Intravenous injection of normal saline 5 mL

Sponsors

The Second Xiangya Hospital of the Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-60 years; 2. 18 kg/m2 < BMI < 28 kg/m2; 3. End-stage renal disease caused by chronic glomerulonephritis; 4. Patients receiving brain dead donor kidney transplantation; 5. Pleco complex gene was detected as heterozygous; 6. High compliance.

Exclusion criteria

Exclusion criteria: 1. ESRD caused by secondary diseases, such as hypertension and diabetes; 2. There are local or systemic infections of the lung, urogenital tract, etc.; 3. Hemoglobin greater than 130 g/L and less than 80 g/L; 4. For poorly controlled hypertension, the systolic blood pressure was still greater than 160 mmHg and the diastolic blood pressure was greater than 100 mmHg after oral administration of antihypertensive drugs; 5. Previous history of thromboembolism (cerebral infarction, pulmonary embolism and other deep vein thrombosis); 6. Severe hypercoagulability or other diseases of the blood system; 7. High risk of cardiovascular and cerebrovascular diseases (acute coronary syndrome in the past 6 months); 8. History of malignant tumor in recent two years; 9. Other conditions that are not suitable for participating in this subject (such as pregnancy, mental illness, etc.).

Design outcomes

Primary

MeasureTime frame
Glomerular filtration rate, eGFR;T cells and their subsets by flow cytometry;

Secondary

MeasureTime frame
Length of stay in hospital;Delayed graft function;Hemoglobin concentration;C-reactive protein;Urea nitrogen;Serum creatinine;Creatinine clearance;Renal injury index;

Countries

China

Contacts

Public ContactZheng Dong; Xubiao Xie

Kexing Biopharmaceutical Co., Ltd.

chenguochun@hotmail.com+86 13618463300

Outcome results

None listed

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