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NCT06030843RecruitingPhase 2/3

The Treatment Effects of Empagliflozin on Renal Outcomes in Cardiorenal Syndrome Type 1

Source: ClinicalTrials.gov · Last updated 16 Jun 2026

Brief summary (registry, in English)

Effects of Empagliflozin compared with placebo in cardiorenal syndrome type 1, evaluated by MAKE30.

Status (registry)
Recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
200 (estimated)
First submitted
3 Sept 2023
Start date
1 Mar 2025
Primary completion date
30 Nov 2026
Lead sponsor
Chulalongkorn University
NCT number
NCT06030843

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 200
  • From 1 Mar 2025 to the primary completion date, 30 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously received any SGLT2i in the last 3 months before admission

Other illness

  • Cardiac mechanical support (i.e. extracorporeal membrane oxygenation and intra-aortic balloon pump)
  • Acute coronary syndrome
  • Diagnosed with cause of AKI other than cardiorenal syndrome (eg. sepsis, nephrotoxic, dehydration)
  • Heart or kidney transplanted
  • Allergic to any SGLT2i
  • Type 1 diabetes mellitus
  • History of ketoacidosis, including diabetic ketoacidosis
  • Comorbid conditions with an expected survival of less than 1 months such as end-stage liver or heart disease, or uncurable malignancy

Lab values

  • Baseline eGFR ≤ 20 ml/min/1.73m2 with or without dialysis initiated

Other

  • Denied to participate in the study
  • Cardiogenic shock or unstable hemodynamic (systolic blood pressure of at least 100 mmHg or required inotropic support within last 24 hours)
  • Anuria or requiring dialysis or expected to required dialysis within 24 hr
  • Pregnancy

Who the study is looking for

  • Age 18 years or more
  • Hospitalized for the primary diagnosis of acute denovo or decompensated chronic heart regardless of ejection fraction
  • AKI KDIGO any stage or urine NGAL ≥ 150 ng/mL
  • Must be able to be enrolled into the trial ≤ 12 hours of diagnosis of AKI or elevated urine NGAL

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Medicine Chulalongkorn University
Coordinator of this site? Confirm its status
BangkokThailandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.