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Completed Phase 3 Interventional Results available

A Study to Test the Effect of Empagliflozin in Patients Who Are in Hospital for Acute Heart Failure

ClinicalTrials.gov ID: NCT04157751

Public ClinicalTrials.gov record NCT04157751. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 12, 2026, 4:33 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicentre, Randomised, Double-blind, 90-day Superiority Trial to Evaluate the Effect on Clinical Benefit, Safety and Tolerability of Once Daily Oral EMPagliflozin 10 mg Compared to Placebo, Initiated in Patients Hospitalised for acUte Heart faiLure (de Novo or Decompensated Chronic HF) Who Have Been StabilisEd (EMPULSE)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a study in adults who are in hospital for acute heart failure. The purpose of this study is to find out whether starting to take a medicine called empagliflozin soon after first being treated in hospital helps people with acute heart failure. Participants are in the study for about 3 months. At the beginning, participants are still in hospital. Later, they visit the hospital about 3 times and get 1 phone call. Participants are put into 2 groups by chance. One group takes 1 empagliflozin tablet a day. The other group takes 1 placebo tablet a day. Placebo tablets look like empagliflozin tablets but do not contain any medicine. Empagliflozin belongs to a class of medicines known as SGLT-2 inhibitors. It is used to treat type 2 diabetes. During the study, the doctors check whether participants have additional heart failure events like needing to go to the hospital again because of heart failure. The participants answer questions about how their heart failure affects their life. We then compare the results between the empagliflozin and placebo groups. The doctors also regularly check the general health of the participants.

Study identification

NCT ID
NCT04157751
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
530 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 17, 2020
Primary completion
May 27, 2021
Completion
Jun 1, 2021
Last update posted
Jul 18, 2022

2020 – 2021

United States locations

U.S. sites
30
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
University of Southern California Los Angeles California 90033
Cedars-Sinai Medical Center Los Angeles California 90048
University of California Irvine Orange California 92865
The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center Torrance California 90502
Cardiology Associates Research Co. Daytona Beach Florida 32117
University of Florida Health Jacksonville Jacksonville Florida 32209
Grady Memorial Hospital Atlanta Georgia 30303
Methodist Medical Center Peoria Illinois 61603
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
United Hospital Saint Paul Minnesota 55102
University Of Mississippi Medical Center Jackson Mississippi 39216-4505
Saint Luke's Hospital of Kansas City Kansas City Missouri 64111
University of Nebraska Medical Center Omaha Nebraska 68198
Cardiovascular Associates of the Delaware Valley Elmer New Jersey 08318
Jefferson Washington Township Hospital Washington Township New Jersey 08080
Erie County Medical Center Buffalo New York 14215
The DeMatteis Center for Cardiac Research and Education Greenvale New York 11548
Stony Brook Medicine Stony Brook New York 11794
Montefiore Medical Center The Bronx New York 10467
The University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599
North Carolina Heart and Vascular Raleigh North Carolina 27607
University of Oklahoma Oklahoma City Oklahoma 73104
South Oklahoma Heart Research Group Oklahoma City Oklahoma 73135
Ralph H. Johnson VA Medical Center Charleston South Carolina 29401
Vanderbilt University Medical Center Nashville Tennessee 37232
Pharmatex Research Amarillo Texas 79109
Center for Advanced Cardiac Care - Heart Failure Clinic Plano Texas 75093
Inova Fairfax Medical Campus Falls Church Virginia 22042
Sentara Norfolk General Hospital Norfolk Virginia 23507
University of Wisconsin Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 88 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04157751, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 18, 2022 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04157751 live on ClinicalTrials.gov.

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