drugset / Trial / NCT01436747

Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients

NCT01436747

Phase 3 Completed 168 enrolled University Medical Centre Ljubljana Abbott · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The study 'Safety and Efficacy of Paricalcitol for Reduction of Proteinuria in Kidney Transplant Recipients' is designed to assess the effects of paricalcitol in kidney transplant recipients with proteinuria. It is a single centre, randomized, placebo-controlled, double-blind clinical trial that tests the hypothesis that 24 weeks' treatment with paricalcitol compared to placebo will result in a decrease in urinary protein excretion in recipients of a kidney transplant at least three months after transplantation. Additionally, the effects of paricalcitol on albuminuria, estimated glomerular filtration rate, and blood pressure will be investigated.

Timeline

Start
2012-07
Primary completion
2014-10
Completion
2015-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Paricalcitol Other / unclassified 2 ug Oral