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Clinical Trial Details

Trial ID: L0339
Source ID: NCT02672293
Associated Drug: Phoslax
Title: Determining Oral Phosphate Tolerance Across the Spectrum of Glomerular Filtration Rate
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Chronic Kidney Disease
Interventions: DRUG: Phoslax
Outcome Measures: Primary: Fractional excretion of phosphate, Fractional excretion of phosphate will be measured at baseline and at 1 and 2 hours following a standardized oral phosphate challenge, Change in fractional excretion of phosphate at 1 and 2 hours | Secondary: Fibroblast growth factor-23, Biomarker of phosphate homeostasis, Change in level of fibroblast growth factor 23 at 2 hours|Vitamin D, Biomarker of phosphate homeostasis, Change in level of vitamin D and vitamin D metabolites at 2 hours|klotho, Biomarker of phosphate homeostasis, Change in level of circulation kloth at 2 hours
Sponsor/Collaborators: Sponsor: Dr. Rachel Holden
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases:
Enrollment: 78
Study Type: INTERVENTIONAL
Study Designs: Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: OTHER
Start Date: 2013-01
Completion Date: 2018-04-18
Results First Posted:
Last Update Posted: 2022-07-05
Locations: Kingston General Hospital, Kingston, Ontario, K7L 3N6, Canada
URL: https://clinicaltrials.gov/show/NCT02672293