Trial ID: | L1481 |
Source ID: | NCT05713851
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Associated Drug: |
Dapagliflozin
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Title: |
Dapaglifozin to Avoid Acute Kindey Injury (AKI) to Chronic Kidney Disease (CKD) Transition: DAKI-CKD Study
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Acronym: |
DAKI-CKD
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Status: |
RECRUITING
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Study Results: |
NO
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Results: |
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Conditions: |
AKI - Acute Kidney Injury|Biomarkers|Transition to CKD|CKD
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Interventions: |
DRUG: Dapagliflozin
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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
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
PHASE2|PHASE3
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Enrollment: |
100
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: PREVENTION
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Start Date: |
2023-01-01
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Completion Date: |
2025-01-01
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Results First Posted: |
|
Last Update Posted: |
2024-03-05
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Locations: |
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, 14080, Mexico
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URL: |
https://clinicaltrials.gov/show/NCT05713851
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