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Clinical Trial Details

Trial ID: L1481
Source ID: NCT05713851
Associated Drug: Dapagliflozin
Title: Dapaglifozin to Avoid Acute Kindey Injury (AKI) to Chronic Kidney Disease (CKD) Transition: DAKI-CKD Study
Acronym: DAKI-CKD
Status: RECRUITING
Study Results: NO
Results:
Conditions: AKI - Acute Kidney Injury|Biomarkers|Transition to CKD|CKD
Interventions: DRUG: Dapagliflozin
Outcome Measures: Primary: The primary outcome will be the mean change in urinary Serpin A3 (uSerpinA3) levels 18 months after randomization of the patients., 18 months | Secondary: GFR at 18 months of randomization calcutated with CKD-EPI creatinine-Cystatin C Equation., 18 months|Urine HSP-72 levels 18 months after randomization of the patients, 18 months|Urine NGAL levels 18 months after randomization of the patients, 18 months|Urine KIM-1 levels 18 months after randomization of the patients, 18 months|Serum Cystatin C levels 18 months after randomization of the patients, 18 months|Serum creatinine levels 18 months after randomization of the patients, 18 months
Sponsor/Collaborators: Sponsor: Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran | Collaborators: Olynka Vega Vega|Noemi del Toro Cisneros|Miguel Ángel Martínez Rojas
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2|PHASE3
Enrollment: 100
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: PREVENTION
Start Date: 2023-01-01
Completion Date: 2025-01-01
Results First Posted:
Last Update Posted: 2024-03-05
Locations: Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, 14080, Mexico
URL: https://clinicaltrials.gov/show/NCT05713851