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Completed Phase 3 Interventional Results available

Oral Iron Repletion Effects On Oxygen Uptake in Heart Failure

ClinicalTrials.gov ID: NCT02188784

Public ClinicalTrials.gov record NCT02188784. 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 6, 2026, 4:24 AM EDT

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

Brief summary

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

The purpose of this study is to determine if oral iron (Fe) polysaccharide is superior to oral placebo in improving functional capacity as measured by change in peak VO2 (oxygen uptake) by CPET (Cardiopulmonary Exercise Testing) , of a broad population of patients with HFrEF (Heart Failure with Reduced Ejection Fraction) and Fe deficiency at 16 weeks. Hypothesis: In a broad population of HFrEF patients with Fe deficiency, compared to oral placebo, therapy with oral Fe polysaccharide will be associated with improvement in functional capacity at 16 weeks as assessed by CPET.

Study identification

NCT ID
NCT02188784
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Adrian Hernandez
Other
Enrollment
225 participants

Conditions and interventions

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
Sep 2, 2014
Primary completion
Apr 5, 2016
Completion
Apr 5, 2016
Last update posted
Jul 10, 2017

2014 – 2016

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Emory University School of Medicine Atlanta Georgia 30322
Johns Hopkins Hospital Baltimore Maryland 21287
Tufts Medical Center Boston Massachusetts 02111
Massachusetts General Hospital Boston Massachusetts 02114
Brigham and Women's Hospital Boston Massachusetts 02115
Mayo Clinic Rochester Minnesota 55905
Saint Louis University Hospital St Louis Missouri 63110
Washington University School of Medicine St Louis Missouri 63110
Duke University Medical Center Durham North Carolina 27705
University Hospitals-Case Medical Center Cleveland Ohio 44106
Metor Health System Cleveland Ohio 44109
Cleveland Clinic Foundation Cleveland Ohio 44195
Lancaster General Hospital Lancaster Pennsylvania 17603
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104
Thomas Jefferson University Philadelphia Pennsylvania 19107
University of Utah Hospitals and Clinics Murray Utah 84107
The University of Vermont - Fletcher Allen Health Care Burlington Vermont 05401

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02188784, 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 10, 2017 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02188784 live on ClinicalTrials.gov.

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