Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00223054
Other study ID # 004
Secondary ID
Status Completed
Phase Phase 4
First received September 14, 2005
Last updated August 3, 2011
Start date March 2005
Est. completion date October 2006

Study information

Verified date June 2008
Source University of Schleswig-Holstein
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

In this study the researchers want to investigate genetic polymorphisms of cytochrome 450 enzymes and the multiple drug resistance (MDR) gene in renal transplant patients to look for differences in dosing of immunosuppressive drugs (tacrolimus, sirolimus, everolimus, cyclosporine A).

All patients who receive one of these drugs can be included and drug blood trough levels, dosing and genetics are compared.


Description:

Primary endpoint is the

1. serum creatinine in patients with and without polymorphysms

2. rate of rejections in patients with and without polymorphysms


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date October 2006
Est. primary completion date June 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Renal transplant patients receiving one or more of the following drugs:

- tacrolimus

- sirolimus

- everolimus

- cyclosporin A

- fluvastatin

- Informed consent given by the patient

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Drug:
tacrolimus
retrospective analyze of drug levels in comparison to polymorphism
sirolimus
retrospective of drug blood trough levels in comparison to polymorphism of enzymes of drug metabolism
everolimus
retrospective of drug blood trough levels in comparison to polymorphism of enzymes of drug metabolism
cyclosporin A
retrospective of drug blood trough levels in comparison to polymorphism of enzymes of drug metabolism

Locations

Country Name City State
Germany University of Schleswig-Holstein, Campus Kiel, Department of Nephrology Kiel

Sponsors (2)

Lead Sponsor Collaborator
University of Schleswig-Holstein University of Kiel

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Renders L, Frisman M, Ufer M, Mosyagin I, Haenisch S, Ott U, Caliebe A, Dechant M, Braun F, Kunzendorf U, Cascorbi I. CYP3A5 genotype markedly influences the pharmacokinetics of tacrolimus and sirolimus in kidney transplant recipients. Clin Pharmacol Ther — View Citation

See also
  Status Clinical Trial Phase
Completed NCT01443013 - Analysis of Foxp3 and Vimentin Expression in Renal Transplant Recipient N/A
Completed NCT01759862 - Perioperative Aminophylline to Improve Early Kidney Function After a Kidney Transplant N/A
Active, not recruiting NCT01095172 - RituxiMab INDuction in Renal Transplantation Phase 4
Terminated NCT01292525 - Protocol Calcineurin Inhibitor (CNI) Weaning Phase 3