Logo 1 Logo 2

Clinical Trial Details

Trial ID: L0530
Source ID: NCT03023748
Associated Drug: Intravenous Paricalcitol
Title: Intravenous Paricalcitol in Chronic Hemodialysis Patients
Acronym:
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Endstage Renal Disease|Secondary Hyperparathyroidism
Interventions: DRUG: Intravenous Paricalcitol
Outcome Measures: Primary: Change in left ventricular mass index, MRI determined cardiac parameters, 52 weeks and 104 weeks | Secondary: Change in Coronary artery calcium score, Computed tomography determined coronary artery calcium score, 52 and 104 weeks|Change in Aortic stiffness, aortic pulse wave velocity, 52 and 104 weeks|Change in handgrip strength, nutrition and functional parameters, 52 and 104 weeks|Change in Serum albumin, Nutrition parameters, 52 and 104 weeks|Change in serum Calcium and phosphate, Biochemical parameters of CKD-MBD, 52 and 104 weeks|Change in Intact parathyroid hormone, Biochemical parameters of CKD-MBD, 52 and 104 weeks|Change in alkaline phosphatase, biochemical parameters of CKD-MBD, 52 and 104 weeks
Sponsor/Collaborators: Sponsor: The University of Hong Kong | Collaborators: AbbVie
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 30
Study Type: INTERVENTIONAL
Study Designs: Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2011-09
Completion Date: 2018-01
Results First Posted:
Last Update Posted: 2017-01-18
Locations: Queen Mary Hospital and Tung Wah Hospital, Hong Kong, 0000, Hong Kong
URL: https://clinicaltrials.gov/show/NCT03023748