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Comparative efficacy of mizoribine with mycophenolate mofetil for living related kidney transplantation recipients

Comparative efficacy of mizoribine with mycophenolate mofetil for living related kidney transplantation recipients

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074265
Enrollment
Unknown
Registered
2023-08-02
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

Renal transplantation immunosuppression

Interventions

experimental group:Mizoribine
Contrast group:Mycophenolate Mofetil

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) After donor kidney transplantation; 2) Adult recipients aged 18-75 years, regardless of gender; 3) First-time kidney transplant recipients; 4) Voluntarily sign written informed consent.

Exclusion criteria

Exclusion criteria: 1) Multiple organ transplantation; 2) DSA positive patients had ABO incompatibility and PRA>30%; 3) Recipients with active signs of infection; 4) Recipients with leukocyte counts below 3,000/mm3; 5) Pregnant women, breastfeeding women or women who do not wish to use appropriate contraceptive methods during the study period; 6) Patients with severe gastrointestinal diseases and active peptic ulcer disease; 7) suffering from any mental illness; 8) Patients with severe heart disease and abnormal heart function; 9) Subjects who are known to be allergic to the test drug; 10) Recipients judged unsuitable for inclusion by other competent physicians.

Design outcomes

Primary

MeasureTime frame
Incidence of acute rejection;

Secondary

MeasureTime frame
Recipient survival rate;Survival rate of transplanted kidney;

Countries

China

Contacts

Public ContactTAO LIN

West China Hospital, Sichuan University

kidney5@163.com+86 189 8060 2093

Outcome results

None listed

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