drugset / Trial / NCT03023748

Intravenous Paricalcitol in Chronic Hemodialysis Patients

NCT03023748

Phase 4 Unknown 30 enrolled The University of Hong Kong AbbVie · collab
NaSingle-groupOpen-labelTreatment

Summary

This study aims to provide intravenous paritcalcitol treatment for the sick and poor hemodialysis patients with severe secondary hyperparathyroidism (SHPT) resistant to existing vitamin D analogs therapy or with hypercalcemia precluding the use of existing vitamin D analogs. The study aims to evaluate the effect of paricalcitol on control of SHPT, biochemical parameters of chronic kidney disease-mineral bone disease, cardiac parameters, vascular calcification and stiffness parameters and nutrition status in patients receiving chronic hemodialysis treatment.

Timeline

Start
2011-09
Primary completion
2017-12
Completion
2018-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Paricalcitol Other / unclassified 10 ug Intravenous