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Clinical Trial Details

Trial ID: L0731
Source ID: NCT01994733
Associated Drug: Calcium Carbonate ( Intensive Phosphate Control)
Title: Two phosphAte taRGets in End-stage Renal Disease Trial (TARGET)
Acronym: TARGET
Status: COMPLETED
Study Results: NO
Results:
Conditions: End-stage Renal Disease
Interventions: DRUG: Calcium carbonate ( Intensive phosphate control)|DRUG: Calcium carbonate (Liberalized phosphate control)
Outcome Measures: Primary: Serum phosphate concentration, 26 weeks | Secondary: Number of patients who successfully achieved target serum P at week 26 based on the arm to which they were randomized, 26 weeks|Treatment compliance as defined by taking the study medication at least 80% of the time, 26 weeks|Number of serious adverse events, 26 weeks|Number of hospitalizations for vascular reasons that are unrelated to dialysis access, 26 weeks|Proportion of patients with a vascular death or non-fatal vascular event, 26 weeks|Proportion of patients developing serum calcium > 2.60 mmol/L, 26 weeks|Number of fractures, 26 weeks|Number of patients developing calcific uremic arteriolopathy (ie, calciphylaxis), 26 weeks|Change in quality-of-life, 26 weeks
Sponsor/Collaborators: Sponsor: Unity Health Toronto | Collaborators: Canadian Institutes of Health Research (CIHR)
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 104
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2014-01
Completion Date: 2015-04
Results First Posted:
Last Update Posted: 2015-06-23
Locations: Foothills Medical Centre, Calgary, Alberta, T2N 2T9, Canada|Capital District Health Authority, Halifax, Nova Scotia, B3H 1V7, Canada|St. Joseph's Healthcare, Hamilton, Ontario, L8N 4A6, Canada|London Health Sciences Centre, London, Ontario, N6G 2V4, Canada|St. Michael's Hospital, Toronto, Ontario, M5B 1W8, Canada
URL: https://clinicaltrials.gov/show/NCT01994733