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Iron Deficiency In Pulmonary Hypertension

Primary Purpose

Idiopathic Pulmonary Arterial Hypertension

Status
Unknown status
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Ferricarboxymaltose
Sponsored by
Amsterdam UMC, location VUmc
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Pulmonary Arterial Hypertension focused on measuring Pulmonary arterial hypertension, Iron deficiency, Exercise

Eligibility Criteria

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

Inclusion Criteria:

  • Stable idiopathic pulmonary arterial hypertension (stable disease for at least 3 months)
  • iron deficiency (serum iron below 10 μmol/l, decreased transferrin saturation (< 15% in females and < 20% in males) and serum ferritin < 100 μg/l) irrespective of the coexistence of anaemia

Exclusion Criteria:

  • Current iron therapy (oral or iv)
  • Current other study medication for PAH
  • History of anaemia or current treatment for anaemia
  • Liver function impairment
  • Chronic disease other than PAH (rheumatism, asthma, chronic infection)
  • Acute infection

Sites / Locations

  • VUmcRecruiting

Outcomes

Primary Outcome Measures

six-minute walking distance
The primary endpoint is improvement in six-minute walking distance

Secondary Outcome Measures

Serum iron parameters
Serum iron parameters and inflammatory parameters are measured
Exercise capacity
Cardiopulmonary exercise testing is performed to measure maximal exercise capacity and exercise endurance time.
Quadriceps muscle function
A biopsy from the quadriceps muscle is taken for histochemical analysis, myoglobin measurements and muscle fiber strength characteristics
Cardiac Function
A cardiac MRI is performed to measure cardiac function
Quality of life
Quality of life and NYHA functional class is established.

Full Information

First Posted
February 1, 2011
Last Updated
February 1, 2011
Sponsor
Amsterdam UMC, location VUmc
Collaborators
Vifor Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT01288651
Brief Title
Iron Deficiency In Pulmonary Hypertension
Official Title
Intravenous Iron Treatment In Iron Deficient Patients With Idiopathic Pulmonary Arterial Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
January 2011
Overall Recruitment Status
Unknown status
Study Start Date
January 2011 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
January 2013 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Amsterdam UMC, location VUmc
Collaborators
Vifor Pharma

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with idiopathic pulmonary arterial hypertension (IPAH) and iron deficiency were previously shown to have a decreased six-minute walking distance. Therefore the investigators hypothesized that intravenous iron administration would improve exercise capacity in iron deficient IPAH patients. 30 patients will be recruited for iron infusions. At baseline and after 12 weeks (endpoint)exercise test will be performed.
Detailed Description
Background: Patients with pulmonary arterial hypertension (PAH) develop progressive right heart failure which eventually will lead to death. During progression of the disease the physical performance of the patients deteriorates. Maintaining their exercise capacity is a major goal in PAH treatment. Iron treatment is known to have a positive effect on physical performance in patients with left heart failure and iron deficiency. Whether this is also effective in patients with right heart failure (PAH) and iron deficiency is until now unknown. Objective: To evaluate the effects of intravenous iron supplementation on exercise capacity in iron deficient IPAH patients. Study design: Intervention study Study population: Patients with idiopathic pulmonary arterial hypertension (IPAH) and iron deficiency Patients receive an iron bolus infusion of 1000 mg iron after baseline measurements. Main study parameters/endpoints: Primary endpoint: six minute walking distance (6WMD) Secondary endpoints: cardiopulmonary exercise test, myoglobin concentration in quadriceps muscle, quadriceps muscle fiber strength, serum iron parameters, serum inflammatory parameters, quality of life (QOL), and NYHA functional class. The patients will be hospitalised two days at the beginning and two days at the end of the study to perform the exercise and strength tests, six minute walking distance and for biopsy of the quadriceps muscle. Also NYHA functional class will be determined and a QOL questionnaire has to be filled in. After the baseline measurements an iron infusion will be given (Ferinject 1000mg). The investigators hypothesize that iron deficient IPAH patients will benefit from iron treatment with improved exercise capacity reflected in an increased 6MWD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Pulmonary Arterial Hypertension
Keywords
Pulmonary arterial hypertension, Iron deficiency, Exercise

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Ferricarboxymaltose
Intervention Description
Ferricarboxymaltose (Ferinject®, Vifor Pharma) is used for intravenous iron administration. This iron is administered in high dose iron infusion of 1000 mg iron (equals 20 ml Ferinject) in 250 ml saline in the vein (infusion site)within 2 hours. During infusion, patients will be observed and blood pressure and heart rate are monitored before and after administration. Four weeks after iron administration, iron parameters are measured in the general practitioners setting. When iron parameters are still under normal values, a repeat infusion will be given of 500 mg iron (equals 10 ml Ferinject).
Primary Outcome Measure Information:
Title
six-minute walking distance
Description
The primary endpoint is improvement in six-minute walking distance
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Serum iron parameters
Description
Serum iron parameters and inflammatory parameters are measured
Time Frame
0 and 12 weeks
Title
Exercise capacity
Description
Cardiopulmonary exercise testing is performed to measure maximal exercise capacity and exercise endurance time.
Time Frame
0 and 12 weeks
Title
Quadriceps muscle function
Description
A biopsy from the quadriceps muscle is taken for histochemical analysis, myoglobin measurements and muscle fiber strength characteristics
Time Frame
0 and 12 weeks
Title
Cardiac Function
Description
A cardiac MRI is performed to measure cardiac function
Time Frame
0 and 12 weeks
Title
Quality of life
Description
Quality of life and NYHA functional class is established.
Time Frame
0 and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Stable idiopathic pulmonary arterial hypertension (stable disease for at least 3 months) iron deficiency (serum iron below 10 μmol/l, decreased transferrin saturation (< 15% in females and < 20% in males) and serum ferritin < 100 μg/l) irrespective of the coexistence of anaemia Exclusion Criteria: Current iron therapy (oral or iv) Current other study medication for PAH History of anaemia or current treatment for anaemia Liver function impairment Chronic disease other than PAH (rheumatism, asthma, chronic infection) Acute infection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gerrina Ruiter, MD
Phone
+31 20 444 4915
Email
G.Ruiter@vumc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Anton Vonk-Noordegraaf, Prof MD PhD
Phone
+31 20 444 4710
Email
A.Vonk@vumc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anton Vonk-Noordegraaf, Prof MD PhD
Organizational Affiliation
VU University Medical Center, Deparment of Pulmonology
Official's Role
Principal Investigator
Facility Information:
Facility Name
VUmc
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gerrina Ruiter, MD
Phone
+31 20 444 4915
Email
G.Ruiter@vumc.nl
First Name & Middle Initial & Last Name & Degree
Anton Vonk Noordegraaf, Prof MD PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
26401247
Citation
Ruiter G, Manders E, Happe CM, Schalij I, Groepenhoff H, Howard LS, Wilkins MR, Bogaard HJ, Westerhof N, van der Laarse WJ, de Man FS, Vonk-Noordegraaf A. Intravenous iron therapy in patients with idiopathic pulmonary arterial hypertension and iron deficiency. Pulm Circ. 2015 Sep;5(3):466-72. doi: 10.1086/682217.
Results Reference
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Iron Deficiency In Pulmonary Hypertension

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