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Completed Phase 3 Interventional Results available

DETERMINE-reduced - Dapagliflozin Effect on Exercise Capacity Using a 6-minute Walk Test in Patients With Heart Failure With Reduced Ejection Fraction

ClinicalTrials.gov ID: NCT03877237

Public ClinicalTrials.gov record NCT03877237. 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 29, 2026, 5:19 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

International, Multicentre, Parallel-group, Randomised, Double-blind, Placebo-controlled, Phase III Study Evaluating the Effect of Dapagliflozin on Exercise Capacity in Heart Failure Patients With Reduced Ejection Fraction

Brief summary

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

International, Multicentre, Parallel-group, Randomised, Double-blind, Placebo-controlled, Phase III Study Evaluating the effect of Dapagliflozin on Exercise Capacity in Heart Failure Patients with Reduced Ejection Fraction (HFrEF)

Study identification

NCT ID
NCT03877237
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
313 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 150 Years
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
Apr 8, 2019
Primary completion
Mar 6, 2020
Completion
Mar 6, 2020
Last update posted
May 4, 2021

2019 – 2020

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Research Site Alexander City Alabama 35010 —
Research Site Fairhope Alabama 36532 —
Research Site Fort Payne Alabama 35967 —
Research Site Mobile Alabama 36608 —
Research Site Beverly Hills California 90211 —
Research Site Torrance California 90502 —
Research Site Stamford Connecticut 06905 —
Research Site Miami Florida 33133 —
Research Site Miami Florida 33173 —
Research Site Tucker Georgia 30084 —
Research Site Munster Indiana 46321 —
Research Site Petoskey Michigan 49770 —
Research Site Kansas City Missouri 64111 —
Research Site New Brunswick New Jersey 08901 —
Research Site Buffalo New York 14215 —
Research Site New York New York 10001 —
Research Site Rosedale New York 11422 —
Research Site Burlington North Carolina 27215 —
Research Site Abington Pennsylvania 19001 —
Research Site Pittsburgh Pennsylvania 15212 —
Research Site Tullahoma Tennessee 37388 —
Research Site Falls Church Virginia 22042 —
Research Site Seattle Washington 98101 —

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 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03877237, 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 May 4, 2021 · Synced Sep 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03877237 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →