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Effects of IV Iron Replacement on Exercise Capacity in Individuals With Heart Failure

Primary Purpose

Heart Failure, Iron-deficiency

Status
Enrolling by invitation
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
IV Iron Infusion Group
Sponsored by
Radha Gopalan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Reduced ejection fraction, Exercise, iron supplementation, Cardiopulmonary exercise, peak oxygen uptake

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 18-90 years New York Heart Association Class II-III heart failure Left ventricular dysfunction with left ventricular ejection fraction ≤ 40% Ferritin < 100 ng/mL or 100-300 ng/mL with transferrin saturation (TSAT) < 20% Patients deemed by an attending physician to require intravenous iron therapy The patient is willing and able to comply with the protocol and has provided written informed consent Exclusion Criteria: Iron overload disorders or allergy, concomitant nutritional deficiencies- B12 and folate Recent Acute Coronary Syndrome Physical barriers to exercise capacity Currently presenting in heart failure exacerbation Declined participation Chronic liver disease NYHA class IV Active bleeding Pregnancy Life expectancy ≤ 12 months

Sites / Locations

  • Banner - University Medical Center, Phoenix campus

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

IV Iron Infusion Group

Control Group

Arm Description

Subjects will receive iron infusion 1 week after enrollment. Dosage of iron will be at discretion of physicians

Subjects will not receive iron replacement infusion.

Outcomes

Primary Outcome Measures

Exercise Capacity
Cardiopulmonary exercise testing will be administered to measure Peak V02. During the exercise testing a special mouthpiece that can measure oxygen and carbon dioxide is used to measure peak oxygen uptake.
Patient subjective outcome measures
Subjects will complete the Kansas City Cardiomyopathy Questionnaire.The lowest score is 0 and the highest score is 100. The higher the score is, the better the quality of life.

Secondary Outcome Measures

Objective Quality of Life measures
A 6-minute walk test will be administered to determine if the NYHA class has improved.

Full Information

First Posted
March 31, 2023
Last Updated
July 28, 2023
Sponsor
Radha Gopalan
Collaborators
American Regent, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05816265
Brief Title
Effects of IV Iron Replacement on Exercise Capacity in Individuals With Heart Failure
Official Title
Effects of IV Iron Replacement on Exercise Capacity in Individuals With Heart Failure With Reduced Ejection Fraction and Iron Deficiency
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
August 2023 (Anticipated)
Primary Completion Date
March 2025 (Anticipated)
Study Completion Date
March 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Radha Gopalan
Collaborators
American Regent, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with heart failure with reduced ejection fraction and iron deficiency will be randomized to either receive iron infusion or be in the control group. The study is looking at how iron replacement affects exercise capacity as measured by peak oxygen uptake.
Detailed Description
Currently 5.7 million people in the United States (US) have Heart Failure and it is expected that by 2030 more than 8 million people will have this condition, accounting for a 46 % increase in prevalence. Iron deficiency and anemia are both common findings in patients with heart failure and contribute to morbidity and mortality. The average cost of hospital admissions for heart failure are about $17,000-25,000; creating a large burden on health-care resources and iron replacement may serve to reduce readmissions at less than a tenth of the cost. The working hypothesis to support Iron supplementation is that it improves oxygen carrying capacity, thereby improving exercise tolerance. Exercise tolerance in patients with heart failure is an important prognostic indicator. Role of iron supplementation has been investigated to improve quality of life and outcomes in patients with heart failure and two large multi-centric trails. FAIR-HF and CONFIRM-HF have both showed significant improvement in symptoms and six-minute walk distances in patients with HFrEF after IV iron supplementation. This was found to be true for both anemic and non-anemic patients. Despite the current data, IV iron supplementation is currently only a class IIb recommendation for HFrEF and routine testing of iron studies, is not a part of practice guidelines for heart failure management. Part of what makes the existing data less compelling is that exercise tolerance was assessed using a 6-minute walk test and though it correlates with functional capacity, it is a sub-maximal exercise test and cannot assess the peak oxygen uptake. Individuals with heart failure are often unable to attain this peak oxygen uptake. The inability to increase O2 uptake with exercise is what affects exercise capacity. The study aims to bridge the gap between the response seen after IV iron supplementation and the change in physiology we attribute to it using a formal Cardiopulmonary exercise testing. A peak VO2 provides the most objective assessment of functional capacity in patients with HF. This parameter is a surrogate marker for the maximal cardiac output that an individual can achieve. A modest increase in peak VO2 of 6% at 3 months of exercise training has been associated with a reduction in mortality by 5 %.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Iron-deficiency
Keywords
Reduced ejection fraction, Exercise, iron supplementation, Cardiopulmonary exercise, peak oxygen uptake

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomization will be 1:1 between control group and iron group. Subjects randomized to the iron group will receive iron infusion 1 week after enrollment. The control group will not receive iron replacement infusion.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IV Iron Infusion Group
Arm Type
Experimental
Arm Description
Subjects will receive iron infusion 1 week after enrollment. Dosage of iron will be at discretion of physicians
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Subjects will not receive iron replacement infusion.
Intervention Type
Drug
Intervention Name(s)
IV Iron Infusion Group
Other Intervention Name(s)
Ferric carboxymaltose injection
Intervention Description
Subjects will receive IV Iron Infusion. Dosage of iron will be at discretion of physicians
Primary Outcome Measure Information:
Title
Exercise Capacity
Description
Cardiopulmonary exercise testing will be administered to measure Peak V02. During the exercise testing a special mouthpiece that can measure oxygen and carbon dioxide is used to measure peak oxygen uptake.
Time Frame
2 months after IV iron infusion
Title
Patient subjective outcome measures
Description
Subjects will complete the Kansas City Cardiomyopathy Questionnaire.The lowest score is 0 and the highest score is 100. The higher the score is, the better the quality of life.
Time Frame
2 months after IV iron infusion
Secondary Outcome Measure Information:
Title
Objective Quality of Life measures
Description
A 6-minute walk test will be administered to determine if the NYHA class has improved.
Time Frame
2 months after IV iron infusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-90 years New York Heart Association Class II-III heart failure Left ventricular dysfunction with left ventricular ejection fraction ≤ 40% Ferritin < 100 ng/mL or 100-300 ng/mL with transferrin saturation (TSAT) < 20% Patients deemed by an attending physician to require intravenous iron therapy The patient is willing and able to comply with the protocol and has provided written informed consent Exclusion Criteria: Iron overload disorders or allergy, concomitant nutritional deficiencies- B12 and folate Recent Acute Coronary Syndrome Physical barriers to exercise capacity Currently presenting in heart failure exacerbation Declined participation Chronic liver disease NYHA class IV Active bleeding Pregnancy Life expectancy ≤ 12 months
Facility Information:
Facility Name
Banner - University Medical Center, Phoenix campus
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85006
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Only coded research data will be shared for data analysis by study team. Only limited data set may be shared with sponsor if requested according to data agreement. Future use data will be de-identified and stored in REDCap and only utilized by the investigator's department researchers. Publications and reports will be de-identified.
Citations:
PubMed Identifier
20570952
Citation
Jankowska EA, Rozentryt P, Witkowska A, Nowak J, Hartmann O, Ponikowska B, Borodulin-Nadzieja L, Banasiak W, Polonski L, Filippatos G, McMurray JJ, Anker SD, Ponikowski P. Iron deficiency: an ominous sign in patients with systolic chronic heart failure. Eur Heart J. 2010 Aug;31(15):1872-80. doi: 10.1093/eurheartj/ehq158. Epub 2010 Jun 21. Erratum In: Eur Heart J. 2011 May;32(9):1054.
Results Reference
background
PubMed Identifier
30553903
Citation
von Haehling S, Ebner N, Evertz R, Ponikowski P, Anker SD. Iron Deficiency in Heart Failure: An Overview. JACC Heart Fail. 2019 Jan;7(1):36-46. doi: 10.1016/j.jchf.2018.07.015. Epub 2018 Dec 12.
Results Reference
background
PubMed Identifier
24064572
Citation
Ebner N, von Haehling S. Iron deficiency in heart failure: a practical guide. Nutrients. 2013 Sep 23;5(9):3730-9. doi: 10.3390/nu5093730.
Results Reference
background
PubMed Identifier
19920054
Citation
Anker SD, Comin Colet J, Filippatos G, Willenheimer R, Dickstein K, Drexler H, Luscher TF, Bart B, Banasiak W, Niegowska J, Kirwan BA, Mori C, von Eisenhart Rothe B, Pocock SJ, Poole-Wilson PA, Ponikowski P; FAIR-HF Trial Investigators. Ferric carboxymaltose in patients with heart failure and iron deficiency. N Engl J Med. 2009 Dec 17;361(25):2436-48. doi: 10.1056/NEJMoa0908355. Epub 2009 Nov 17.
Results Reference
background
PubMed Identifier
12538418
Citation
Ezekowitz JA, McAlister FA, Armstrong PW. Anemia is common in heart failure and is associated with poor outcomes: insights from a cohort of 12 065 patients with new-onset heart failure. Circulation. 2003 Jan 21;107(2):223-5. doi: 10.1161/01.cir.0000052622.51963.fc.
Results Reference
background
PubMed Identifier
23537975
Citation
Klip IT, Comin-Colet J, Voors AA, Ponikowski P, Enjuanes C, Banasiak W, Lok DJ, Rosentryt P, Torrens A, Polonski L, van Veldhuisen DJ, van der Meer P, Jankowska EA. Iron deficiency in chronic heart failure: an international pooled analysis. Am Heart J. 2013 Apr;165(4):575-582.e3. doi: 10.1016/j.ahj.2013.01.017. Epub 2013 Feb 22.
Results Reference
background
PubMed Identifier
21903058
Citation
Okonko DO, Mandal AK, Missouris CG, Poole-Wilson PA. Disordered iron homeostasis in chronic heart failure: prevalence, predictors, and relation to anemia, exercise capacity, and survival. J Am Coll Cardiol. 2011 Sep 13;58(12):1241-51. doi: 10.1016/j.jacc.2011.04.040.
Results Reference
background
PubMed Identifier
25278814
Citation
Lim EA, Sohn HS, Lee H, Choi SE. Cost-utility of ferric carboxymaltose (Ferinject(R)) for iron-deficiency anemia patients with chronic heart failure in South Korea. Cost Eff Resour Alloc. 2014 Sep 10;12:19. doi: 10.1186/1478-7547-12-19. eCollection 2014.
Results Reference
background
PubMed Identifier
20964473
Citation
Wang G, Zhang Z, Ayala C, Wall HK, Fang J. Costs of heart failure-related hospitalizations in patients aged 18 to 64 years. Am J Manag Care. 2010 Oct;16(10):769-76.
Results Reference
background
PubMed Identifier
18672162
Citation
Fang J, Mensah GA, Croft JB, Keenan NL. Heart failure-related hospitalization in the U.S., 1979 to 2004. J Am Coll Cardiol. 2008 Aug 5;52(6):428-34. doi: 10.1016/j.jacc.2008.03.061.
Results Reference
background
PubMed Identifier
22773109
Citation
Swank AM, Horton J, Fleg JL, Fonarow GC, Keteyian S, Goldberg L, Wolfel G, Handberg EM, Bensimhon D, Illiou MC, Vest M, Ewald G, Blackburn G, Leifer E, Cooper L, Kraus WE; HF-ACTION Investigators. Modest increase in peak VO2 is related to better clinical outcomes in chronic heart failure patients: results from heart failure and a controlled trial to investigate outcomes of exercise training. Circ Heart Fail. 2012 Sep 1;5(5):579-85. doi: 10.1161/CIRCHEARTFAILURE.111.965186. Epub 2012 Jul 6.
Results Reference
background

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Effects of IV Iron Replacement on Exercise Capacity in Individuals With Heart Failure

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