Effect of Intravenous Iron (Ferinject®) on Exercise Capacity and Quality of Life of Stable COPD Patients

NCT ID: NCT02416778

Last Updated: 2016-09-28

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-02-28
• Study Completion Date: 2017-02-28

Brief Summary

Disordered iron metabolism characterizes an important determinant of impaired exercise tolerance and work capacity. Iron-deficiency anemia commonly features impaired aerobic capacity caused by decreased oxygen carrying capacity, and has been associated with a negative effect on dyspnea and walking distance.

Apart from that, iron deficiency without anemia was shown to affect endurance and energetic efficiency via decreased tissue oxidative capacity. Consequently, depleted iron stores could be capable of causing fatigue, breathlessness and impaired exercise tolerance, which are common features of chronic cardiopulmonary diseases like chronic heart failure (CHF) and COPD (Chronic Obstructive Pulmonary Disease). Indeed, a current surge of interest aimed at potential underlying determinants in CHF and COPD independent of the primarily disordered organ.

Recent studies identified iron deficiency without anemia as an independent factor of reduced exercise intolerance in CHF as well as in COPD. Moreover, intravenous iron application significantly improved exercise capacity in CHF patients with iron deficiency in presence as well as in absence of anemia. Comparable to CHF, the daily living of patients with COPD is compromised by impaired exercise tolerance.

However, airflow limitation, as the foremost characteristic of COPD shows only weak associations with exercise capacity. In line with that, exercise capacity showed no remarkable improvement in lung transplant recipients, underlining the presence of systemic determinants of limited exercise tolerance like iron deficiency. The investigators showed that iron deficiency is present in 50% of stable COPD patients (unpublished data), which is according to recently published data.

The investigators presume that iron deficiency contributes to limited exercise capacity in COPD patients. Thus, the aim of this study is to determine whether iv iron is associated with increases exercise capacity in COPD.

Therefore the investigators hypothesize that filling up depleted iron storages will increase exercise capacity, measured by the 6-MWT (Minute Walking Test).

Conditions

Pulmonary Disease, Chronic Obstructive

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment Arm

Ferric carboxymaltose, Ferinject® 50mg Iron/ml Solution for Injection / Infusion will be administered in patients with COPD

Group Type: EXPERIMENTAL

Ferric carboxymaltose, Ferinject® 50mg Iron/ml Solution for Injection / Infusion

Intervention Type: DRUG

Interventions

Ferric carboxymaltose, Ferinject® 50mg Iron/ml Solution for Injection / Infusion

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Diagnosis of chronic obstructive pulmonary disease according to the current guidelines
• Evidence of irreversible airflow obstruction on spirometry (i.e. an increase of less than 200ml and 15% in the post-bronchodilator FEV1)
• 30% < FEV1 < 80% predicted
• Stable COPD medication: no dose changes in COPD medication within last 4 weeks
• Age of 40 to 75 years
• Body mass index < 30 kg/m2
• Iron deficiency:

ferritin <100 ng/mL or ferritin 100-300 ng/mL when TSAT (Transferrin saturation) <20%

• Hb between 9.5 and 13.5 g/dL
• MMRC (Modified Medical Research Council Scale) 0 to 3
• Patient must be able to perform the bicycle exercise test according to investigator

Exclusion Criteria

• Meeting contraindications of iv iron administration
• Known active infection
• C-reactive protein>20 mg/L
• clinically significant bleeding
• active malignancy
• History of congestive heart failure
• BNP (Brain Natriuretic Peptide) ≥ 250 pg/ml
• Evidence of myocardial ischemia during Cardiopulmonary Exercise Test (CPET) (i.e. chest pain or signs of ischemia in ECG)
• uncontrolled Hypertension
• other clinical significant chronic heart disease
• Acute myocardial infarction or acute coronary syndrome, transient ischaemic attack or stroke within the last 3 months
• History of peripheral artery occlusive disease
• Typical claudication
• Anaemia due to reasons other than iron deficiency (e.g.haemoglobinopathy)
• History of erythropoietin, i.v. or oral iron therapy, and blood transfusion in previous 12 weeks and/or such therapy planned within the next 6 months
• Immunosuppressive therapy or renal dialysis
• ALT (Alanine Aminotransferase) or AST (Aspartate Aminotransferase) >3times upper limit of normal
• Hemochromatosis
• Significant lung diseases other than COPD
• pulmonary hypertension (maximum of velocity tricuspid regurgitation > 2,8m/sec)
• Exacerbation within prior 4 weeks
• > 1 exacerbation within last year
• bronchoscopic lung volume reduction (BLVR)
• Malignancy within the past 5 years
• Autoimmune diseases
• Rheumatoid diseases
• Chronic renal failure (defined through: eGFR (Estimated Glomerular Filtration Rate) < 60 ml/min)
• Active diet
• Physical rehabilitation training
• Pregnancy, breast feeding
• Participation in other therapeutic trial

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Georg-Christian Funk

OTHER

Sponsor Role: lead

Responsible Party

Georg-Christian Funk

M.D., Assoc. Prof.

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Georg-Christian Funk, M.D.Ass.Prof

Role: PRINCIPAL_INVESTIGATOR

Otto Wagner Spital, Dep. of Respiratory and Critical Care Medicine, Pavillon Hermann, Sanatoriumstr. 2, A-1140 Vienna

Locations

Otto Wagner Spital, Dep. of Respiratory and Critical Care Medicine

Vienna, Vienna, Austria

Site Status: RECRUITING

Countries

Austria

Central Contacts

Georg-Christian Funk, M.D.Ass.Prof

Role: CONTACT

georg-christian.funk@wienkav.at

+43 650 31 00 882

Facility Contacts

Georg-Christian Funk, M.D.

Role: primary

georg-christian.funk@wienkav.at

+43 650 3100882 ext. 882

Other Identifiers

Iron-COPD Pilotstudy

Identifier Type: -

Identifier Source: org_study_id