Logo 1 Logo 2

Clinical Trial Details

Trial ID: L1762
Source ID: NCT02585804
Associated Drug: Dapagliflozin
Title: Treating to Reduce Albuminuria and Normalize Hemodynamic Function in Focal ScLerosis With dApagliflozin Trial Effects
Acronym: TRANSLATE
Status: COMPLETED
Study Results: NO
Results:
Conditions: Focal Segmental Glomerulosclerosis
Interventions: DRUG: Dapagliflozin
Outcome Measures: Primary: The change in Glomerular Filtration Rate (GFR) After an 8 week treatment with dapagliflozin, Glomerular Filtration Rate (GFR, based on plasma inulin clearance) will be measured at baseline and after 8 weeks of treatment., Before and after an 8 week treatment with dapagliflozin | Secondary: The change in Effective Renal Plasma Flow (ERPF) After an 8 week treatment with dapagliflozin, Effective Renal Plasma Flow (ERPF, based on paraaminohippurate plasma clearance) will be measured at baseline and after 8 weeks of treatment., Before and after an 8 week treatment with dapagliflozin|The change in Blood Pressure After an 8 week treatment with dapagliflozin, Before and after 8 weeks of treatment with dapagliflozin|The change in albuminuria after 8 weeks of treatment with dapagliflozin, Before and after 8 weeks of treatment with dapagliflozin|The change in urinary vasoactive mediators after 8 weeks of treatment with dapagliflozin, Before and after 8 weeks of treatment with dapagliflozin
Sponsor/Collaborators: Sponsor: University Health Network, Toronto | Collaborators: AstraZeneca|University of Toronto|Toronto General Hospital
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 10
Study Type: INTERVENTIONAL
Study Designs: Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2015-09
Completion Date: 2017-04-24
Results First Posted:
Last Update Posted: 2018-01-16
Locations: Renal Physiology Laboratory, University Health Network, Toronto, Ontario, M5G 2N2, Canada
URL: https://clinicaltrials.gov/show/NCT02585804