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Efficacy and safety of tocilizumab for renal ischemia-reperfusion: an exploratory study

Efficacy and safety of tocilizumab for renal ischemia-reperfusion: an exploratory study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069721
Enrollment
Unknown
Registered
2023-03-24
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Kidney transplant

Interventions

Test group:Tocilizumab
Control group:Normal saline

Sponsors

Renji Hospital affiliated to Shanghai Jiao Tong University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Subjects have given written consent to participate in the study 2. Renal transplantation in our hospital with regular follow-up 3. Patient sex not restricted, age = 18 years 4. Subjects previously known to have covid-19 must meet the following criteria: be asymptomatic for at least 1 month prior to initiation of screening 5. Donor kidneys receiving DCD, DBD, DBCD donations

Exclusion criteria

Exclusion criteria: 1) Multiple organ transplant recipients 2) Active viral infections such as BK virus (BKV) cytomegalovirus (CMV), EBV, hepatitis B virus (HBV) or hepatitis C virus (HCV) infection 3) Severe infection is occurring or has a history of infection requiring hospitalization 4) Active TB or latent TB 5) Liver function tests were abnormal: alanine aminotransferase (ALT), aspartate aminotransferase (AST) > 2.0 × the upper limit of normal, bilirubin > 1.5 × the upper limit of normal 6) Neutropenia (< 2 x109 / L) or thrombocytopenia (< 100 x109 / L) 7) History of diverticulitis, inflammatory bowel disease or gastrointestinal perforation 8) Serious medical or psychiatric disorders that, according to the investigator, could interfere with participation in the study 9) Current or recent (within the last 3 months) participation in another clinical drug trial 10) Living kidney transplant recipients 11) Other conditions that the investigator considered unsuitable for enrollment

Design outcomes

Primary

MeasureTime frame
Scr;DGF;

Secondary

MeasureTime frame
cfDNA;Urine protein;complement;Inflammatory indicators;

Countries

China

Contacts

Public ContactZhang Ming

Renji Hospital affiliated to Shanghai Jiao Tong University Medical College

15736875970@163.com+86 21 53882042

Outcome results

None listed

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