Randomized Clinical Study to Analyse the Effects of Dapagliflozin on Renal Morphology and Renal Perfusion in Patients With Impaired Renal Function One Year After Kidney Transplantation

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The aim of this study is to observe the mechanisms of dapagliflozin on the renal interstitial tissue and renal perfusion. For this purpose, renal transplanted patients as an excellent model of CKD and high cardiovascular risk (similar to patients in DAPA-CKD study) are included in this study. The objectives of the study are to analyze the effects of dapagliflozin on renal morphology and renal perfusion in patients with impaired renal function one year after kidney transplantation. This is a randomized (1:1), single centre clinical study. Each patient will be randomly assigned in an unblinded fashion to 10 mg Dapagliflozin or not 9 months after transplantation. At least 48 patients will be randomized and included. The routine renal biopsy taken one year after kidney transplantation will allow us to determine the morphological integrity of peritubular fibroblasts, interstitial inflammatory cell density and investigate markers of inflammation, oxidative stress and nitic oxide synthase expression (iNOS).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Female and male patients aged between 18 and 75 years

• Patients with renal transplant having a stable eGFR, who are in stable condition, 9 months after transplantation, irrespective of their diabetes status

• Females of child bearing potential must be using adequate contraceptive precautions

• Females of childbearing potential or within two years of the menopause must have a negative urine pregnancy test at screening visit

• Informed consent (§ 40 Abs. 1 Satz 3 Punkt 3 AMG) has to be given in written form

Locations
Other Locations
Germany
Clinical Research Center (CRC)
RECRUITING
Erlangen
Time Frame
Start Date: 2023-07-28
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 48
Treatments
Active_comparator: Dapagliflozin
Dapagliflozin + standard of care
No_intervention: Standard of care
standard of care only
Related Therapeutic Areas
Sponsors
Leads: University of Erlangen-Nürnberg Medical School

This content was sourced from clinicaltrials.gov