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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 Oct 29, 2026, 7:13 PM 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 3, 2014 (Actual)
Primary completion
Apr 6, 2016 (Actual)
Completion
Apr 6, 2016 (Actual)
Last update posted
Jul 11, 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 11, 2017 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02188784 live on ClinicalTrials.gov.

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