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Efficacy and safety of mycophenolate sodium enteric coated tablets after living donor kidney transplantation

Efficacy and safety of mycophenolate sodium enteric coated tablets after living donor kidney transplantation

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121665
Enrollment
Unknown
Registered
2026-04-01
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Kidney transplant

Interventions

intervention group:All subjects received domestic mycophenolate sodium enteric coated tablets (EC-MPS, ruiyirong)+standard immunosuppressive therapy.

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.18-65 years old, regardless of gender; 2.He was diagnosed with end-stage renal disease and received living donor kidney transplantation; 3.It is planned to use domestic mycophenolate sodium enteric coated tablets (EC-MPS, ruiyirong) as one of the immunosuppressive regimens after operation; 4.The preoperative evaluation was consistent with the indications of transplantation, and there were no serious complications; 5.They signed the informed consent and were willing to participate in the study and complete the follow-up.

Exclusion criteria

Exclusion criteria: 1.Allergic history to domestic mycophenolate sodium enteric coated tablets (EC-MPS, ruiyirong) or other related drugs; 2.Previous severe cardiovascular, liver or other systemic diseases affected the prognosis; 3.Other experimental treatments were needed after operation; 4.Pregnant or lactating women; 5.The compliance was poor and the follow-up could not be completed. 6.Other reasons that the researcher determines are not suitable for participating in the study.

Design outcomes

Primary

MeasureTime frame
Incidence of acute rejection within 6 months post-surgery;Renal function parameters;

Countries

China

Contacts

Public ContactDingxiaoming

The First Affiliated Hospital of Xi'an Jiaotong University

dongbq9707@163.com+86 182 9268 2128

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026