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A four-drug combination therapy in living donor renal transplantation

A four-drug combination therapy consisting of low-dose tacrolimus, low-dose mycophenolate mofetil, corticosteroids, mizoribine in living donor renal transplantation: a randomized study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICQ-15007131
Enrollment
Unknown
Registered
2015-08-25
Start date
2012-01-27
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 renal transplantation

Interventions

a four-drug combination therapy :Patients underwent treatment with a four-drug combination therapy consisting of tacrolimus, MMF, corticosteroid mizoribine.
a three -drug combination therapy :Patients underwent treatment with a three-drug combination therapy consisting of tacrolimus, MMF corticosteroid.

Sponsors

Henan Provincial Peoples Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. ABO-identical or compatible living donor renal transplantation; 2. 17 to 60 years of age; 3. No consideration to be given to gender, age, or underlying disease; 4. 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 with white blood cell count <3000/mm3; 4. Patients who have a history of allergies to any investigational product (FK-506, MMF, MZR) or steroids; 5. Cases that have been determined by the study principal study investigators to be unsuitable for administration of the study drugs.

Design outcomes

Primary

MeasureTime frame
The incidence rates of acute rejection;The occurrence of calcineurin inhibitor-induced renal damage;The incidence rates of adverse effects such as diarrhea caused by MMF;

Secondary

MeasureTime frame
the incidence rates of other adverse effects;

Countries

China

Contacts

Public ContactTian-zhong Yan
ytz460@hotmail.com+86 37165580608

Outcome results

None listed

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