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NCT05360615

The Effects of Empagliflozin on Renal Outcomes in Post Severe Acute Kidney Injury Survivors

Active, enrolled Phase 1 Last updated 17 August 2025
What this trial tests

Phase 1 trial testing Empagliflozin 10 MG in Empagliflozin in Post AKI Stage 2-3 in 147 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 July 2022
Primary endpoint
1 June 2024
1 July 2026

Quick facts

Lead sponsorChulalongkorn University
PhasePhase 1
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment147
Start date1 July 2022
Primary completion1 June 2024
Estimated completion1 July 2026
Sites1 location across Thailand

Drugs / interventions tested

Conditions studied

Sponsor

Chulalongkorn University

Who can join

18 and older, any sex, with Empagliflozin in Post AKI Stage 2-3. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Effects of Empagliflozin compared with placebo in post severe acute kidney injury survivors, evaluated by MAKE365.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. SGLT2 Inhibitors and Long-Term Outcomes After AKI.
    Wannakittirat A, Nimkietkajorn V, Thanapongsathorn P, Chaijamorn W, et al · · 2026 · PMID 41684789 · DOI 10.1016/j.ekir.2025.103752
  2. What Are the Impacts of Introducing an SGLT2 Inhibitor after a Recent Episode of Acute Kidney Injury?
    Proença de Moraes T. · · 2024 · PMID 38546982 · DOI 10.34067/kid.0000000000000386

Verify or expand the search:

Other trials of Empagliflozin 10 MG

Trials testing the same drug.

Other Chulalongkorn University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05360615.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing