Logo 1 Logo 2

Clinical Trial Details

Trial ID: L0422
Source ID: NCT03010072
Associated Drug: Low-Dose Sucroferric Oxyhydroxide
Title: The Effect of Phosphate Lowering Using Sucroferric Oxyhydroxide (PA21) on Calcification Propensity of Serum
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Endstage Renal Disease
Interventions: DRUG: low-dose sucroferric oxyhydroxide|DRUG: high-dose sucroferric oxyhydroxide
Outcome Measures: Primary: Propensity of serum for calcification - H1, The primary outcome is change in the mean T50- Test values between different study phases (wash-out/treatment/control)., 10.5 weeks | Secondary: Change in Serum Phosphate, The secondary outcome is the Change of mean Serum Phosphate Levels between different study visits, 10.5 weeks
Sponsor/Collaborators: Sponsor: Prim. Priv. Doz. Dr. Daniel Cejka | Collaborators: Vifor Fresenius Medical Care Renal Pharma
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 40
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: DIAGNOSTIC
Start Date: 2017-06-09
Completion Date: 2019-05-10
Results First Posted:
Last Update Posted: 2019-07-22
Locations: Ordensklinikum Linz GmbH Elisabethinen, Linz, Upper Austria, 4020, Austria
URL: https://clinicaltrials.gov/show/NCT03010072