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Mizoribine Versus Mycophenolate Mofetil after living donor kidney transplantation for Gastrointestinal Symptoms: a retrospective study in China

Mizoribine Versus Mycophenolate Mofetil after living donor kidney transplantation for Gastrointestinal Symptoms: a retrospective study in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ORN-16007878
Enrollment
Unknown
Registered
2016-02-02
Start date
2012-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

living donor kidney transplantation

Interventions

mizoribine group:Patients underwent treatment with combination therapy consisting of tacrolimus, steroid and mizoribineine
mycophenolate mofetil group:Patients underwent treatment with combination therapy consisting of tacrolimus, steroid and mycophenolate mofetil

Sponsors

General Hospital of Chinese People's Armed Police Forces
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. First renal transplant recipients; 2. No consideration to be given to gender, age, or underlying; 3. Patients are willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with serious infections or cardiac diseases; 2. Women who are pregnant or seeking to become pregnant during the study period; 3. Patients who treated with cyclosporine and azathioprine; 4. Patients who have a history of allergies to any investigational product (FK506,MZR,MMF) or steroids.

Design outcomes

Primary

MeasureTime frame
the prevalence of GI Symptom;

Secondary

MeasureTime frame
the prevalence of AR;Clinical findings (index of renal function);

Countries

China

Contacts

Public ContactYi Shi
shiyi_jp@msn.com+86 13552603674

Outcome results

None listed

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