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Completed

NCT Number: NCT00952302

Study of the Effects of Iron Levels on the Lungs at High Altitude

The study hypothesis is that body iron levels are important in determining the increase in lung blood pressure that occurs in response to low oxygen levels. The purpose of this study is to determine whether this is true at high altitude, where oxygen levels are low.

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Key information

About this study

Pulmonary hypertensive disorders frequently complicate hypoxic lung disease and worsen patient survival. Hypoxia-induced pulmonary hypertension is also a major cause of morbidity at high altitude. Hypoxia causes pulmonary hypertension through hypoxic pulmonary vasoconstriction and vascular remodelling. These processes are thought to be regulated at least in part by the hypoxia-inducible factor (HIF) family of transcription factors, which coordinate intracellular responses to hypoxia throughout the body.

HIF is regulated through a cellular degradation process that requires iron as an obligate cofactor. In cultured cells HIF degradation is inhibited by reduction in iron (by chelation with desferrioxamine) and potentiated by iron supplementation. In humans, we have recently shown that, in laboratory experiments lasting 8 hours, acute iron supplementation blunts the pulmonary vascular response to hypoxia, while acute iron chelation with desferrioxamine enhances the response.

This suggests that iron may also affect the pulmonary artery pressure response to hypoxia over longer time periods. The purpose of this study is to investigate this link between iron and the pulmonary artery pressure response to hypoxia, through a study conducted at high altitude allowing concurrent exposure of larger numbers of participants to environmental hypoxia. We wish to explore the extent and the time-course of the effect of iron on pulmonary artery pressure. Cerro de Pascu (4,340 m) in Peru provides the unique ability to make rapid transitions from sea level to high altitude (6-8 hours by road), together with the requisite research facilities. Also, one part of this study involves recruitment of patients with chronic mountain sickness, of whom there are many living in Cerro de Pasco.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

SLR ARM

Inclusion criteria

  • sea level natives of lowland ancestry
  • generally in good health
  • detectable tricuspid regurgitation on echocardiography

Exclusion criteria

  • any significant medical problem
  • known susceptibility to high altitude pulmonary or cerebral oedema
  • taking medications or iron supplements

CMS ARM

Inclusion criteria

  • diagnosis of chronic mountain sickness
  • no recent venesection therapy (within 1 year)
  • detectable tricuspid regurgitation on echocardiography

Exclusion criteria

  • any other significant medical problem

Treatment and study plan

Iron sucrose

Drug

Single intravenous infusion of iron 200 mg

Other names: Venofer

normal saline

Drug

Single intravenous infusion of normal 0.9% saline 100 mls (as placebo)

Venesection

Procedure

Isolvolaemic venesection of total 2 litres of blood - 500 mls each day for 4 days, replaced with normal saline.

Primary outcomes

  1. Change in pulmonary artery systolic pressure

    Time frame: One week (SLR arm) and one month (CMS arm)

Sponsors and collaborators

Lead sponsor

University of Oxford

Other

Collaborators

  • Universidad Peruana Cayetano Heredia

Registry information

Official study title

Physiology Study Investigating the Effects of Supplementation and Depletion of Iron on Hypoxia-related Pulmonary Hypertension

Important dates

Study start
2008
Primary completion
2008
Study completion
2008
First posted
Aug 6, 2009
Registry last updated
Aug 6, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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