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NCT07273838 · ClinicalTrials.gov registry record · Phase 2

Sodium-Glucose Cotransporter-2 Inhibitor for Patients With Acute Cardiorenal Syndrome

A Phase 2 study of Heart Failure and Acute Kidney Injury, sponsored by Yale University.

Recruiting
Registry status
Phase 2
Development phase
130
Enrollment target
2
Study locations

NCT07273838 is a Phase 2 study of Heart Failure and Acute Kidney Injury that is actively recruiting participants, run by Yale University. The registered enrollment target is 130 participants, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (94% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT07273838, a Phase 2 study of Heart Failure and Acute Kidney Injury, is actively recruiting participants, sponsored by Yale University.

RECRUITING
Registry status
Phase 2
Development phase
130 participants
Enrollment target
2
Study locations

Study Summary

The overall objective of this study is to determine whether the addition of SGLT2 inhibitors to usual care in hospitalized patients with heart failure associated acute kidney injury is safe and efficacious. Investigators will assess if SGLT2 inhibition improves a composite cardio-renal outcome (mortality, dialysis, AKI progression, decongestion metrics, heart failure symptoms). Secondary objectives of this study are to compare individual components of the composite outcome as well as changes in biomarkers of kidney injury, inflammation, repair and oxidative stress between those exposed to the SGLT2 inhibitor vs placebo.

Interventions

  • DRUG Placebo
  • DRUG Dapagliflozin 10mg Tab

Study Locations (2)

Connecticut

  • Yale New Haven Hospital-St. Raphael Campus - New Haven
  • Yale New Haven Hospital - New Haven

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2026-03-05
Est. Completion 2029-10-31
Phase Phase 2

Sponsor

Yale University

1,492 total trials

What the Registry Record Tells You About NCT07273838

The ClinicalTrials.gov registry entry for NCT07273838 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (94% lower). The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Heart Failure appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07273838 reports 2 study locations spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT07273838 about?

NCT07273838 is a clinical study titled "Sodium-Glucose Cotransporter-2 Inhibitor for Patients With Acute Cardiorenal Syndrome". The overall objective of this study is to determine whether the addition of SGLT2 inhibitors to usual care in hospitalized patients with heart failure associated acute kidney injury is safe and efficacious. Investigators will assess if SGLT2 inhibition improves a composite cardio-renal outcome (mort...

What is the current status of trial NCT07273838?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 130 participants. The study started on 2026-03-05. Estimated completion is 2029-10-31.

What conditions does trial NCT07273838 study?

This clinical trial studies the following conditions: Heart Failure, Acute Kidney Injury.

What interventions are being tested in trial NCT07273838?

The interventions under investigation include: Placebo (DRUG), Dapagliflozin 10mg Tab (DRUG).

Who is sponsoring clinical trial NCT07273838?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07273838 being conducted?

This trial has 2 study locations across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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