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Efficacy of Mizoribine (MZR) treatment for gastrointestinal symptoms in kidney transplant recipients using mycophenolate mofetil (MMF). - Open-label, multicenter, randomized, controlled trial –

Efficacy of Mizoribine (MZR) treatment for gastrointestinal symptoms in kidney transplant recipients using mycophenolate mofetil (MMF). - Open-label, multicenter, randomized, controlled trial – - Mizoribine Convert Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008649
Enrollment
200
Registered
2012-08-08
Start date
2012-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Kidney transplantation

Interventions

mizoribine mycophenolate mofetil

Sponsors

Tokyo Women Medical University, Dep. Urology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Conduct a GSRS survey during MMF treatment, and patients included if GSRS score 3 (on a scale of 1 to 7) applies to more than 2 items, or GSRS score 4 applies to at least one of the following: (1):Abdominal pain, (2):Heartburn, (10):Decreased passage of stools, (11):Increased passage of stools, (12):Loose stools, (14):Urgent need for defecation. Patients who had a detailed briefing of the trial with explanatory documents prior to the enrollment, and voluntarily signed a consent form.

Exclusion criteria

Exclusion criteria: 1. currently undergoing acute rejection 2. positive for DSA 3. serum creatinine level of less than 3mg/dL 4. a severe infection other than viral infection 5. white blood cell counts of less than 3,000/mm3 6. pregnant women and women suspected of being pregnant 7. aged 19 or younger 8. considered inappropriate by the doctor

Design outcomes

Primary

MeasureTime frame
Difference of GSRS results between the 1st day and a month later.

Countries

Japan

Contacts

Public ContactHideki Ishida

Tokyo Women Medical University Dep. Urology

hishida@kc.twmu.ac.jp03-3353-8111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026