LivingGLP1
Study S002603

Comparative Cardiovascular and Renal Effectiveness and Safety of Empagliflozin and Other SGLT2i in Patients With Type 2 Diabetes (T2D) With and Without Baseline Kidney Disease in the United States

Registration

Registration
NCT05465317
Study type
OBSERVATIONAL
Status
COMPLETED
Enrollment
62197
Start
2022-08-08
Primary completion
2023-05-02
Lead sponsor
Boehringer Ingelheim
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Empagliflozin; DRUG:Dipeptidyl Peptidate-4 inhibitors
Results posted
TRUE
Individual participant data sharing
NO

Registered primary outcomes

  • Incidence Rate of the Composite Outcome Including 40% Decline in Estimated Glomerular Filtration Rate (eGFR), Incident End-stage Renal Disease (ESRD) and All-cause Death [Starting the day after the index date (date of initiation of empagliflozin or DPP4i) and continuing until the first occurrence of the outcome of interest, or end of study date (date of death, date of study end, 2 years after index date). Up to 2 years.]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0004842Kidney and Cardiovascular Effectiveness of SGLT2 Inhibitors vs GLP-1 Receptor Agonists in Type 2 Diabetes.
Edmonston D, Journal of the American College of Cardiology
2024Nonrandomized studyPMID 39142723DOIcites ClinicalTrials.gov:NCT05465317; registry reference DERIVED:39142723