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A retrospective, single-center, noninterventional clinical study of the interaction between tacrolimus and voriconazole in renal transplant recipients

A retrospective, single-center, noninterventional clinical study of the interaction between tacrolimus and voriconazole in renal transplant recipients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048712
Enrollment
Unknown
Registered
2021-07-13
Start date
2021-07-12
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

renal transplantation, invasive fungal infections

Interventions

Test group:No

Sponsors

Second Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Kidney transplant recipients, regardless of gender and older than 18 years old, who received outpatient follow-up or in-patient treatment in the Department of Kidney Transplantation, Second Xiangya Hospital of Central South University; 2.To receive the TAC, Mortimexophenate and Glucocorticoid triple immunosuppressive regimen; 3.Receiving kidney transplantation for the first time; 4.For patients receiving voriconazole in combination, TAC, voriconazole steady state valley concentration data and other relevant clinical data as well as CYP3A4/CYP3A5 genotype should be obtained.

Exclusion criteria

Exclusion criteria: 1. Patients who cannot obtain accurate information on the dosage and main clinical data of tacrolimus and voriconazole; 2. Concomitant use of other immunosuppressants other than the study drug; 3. Plasma exchange therapy was performed during the concentration determination; 4. Patients who are known to be allergic to tacrolimus, mycophenolate mofetil, glucocorticoids, voriconazole or any of the above-mentioned drugs; 5. It is judged by the investigator that it is not suitable to participate in this research.

Design outcomes

Primary

MeasureTime frame
trough concentration;

Countries

China

Contacts

Public ContactYan Miao

Second Xiangya Hospital, Central South University

yanmiao@csu.edu.cn+86 731 85292097

Outcome results

None listed

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