Study of the Effects of Iron Levels on the Lungs at High Altitude
Pulmonary Hypertension, Mountain Sickness
About this trial
This is an interventional basic science trial for Pulmonary Hypertension focused on measuring Hypoxia, Iron, Hypoxia-Inducible Factor 1, Chronic mountain sickness
Eligibility Criteria
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
Sites / Locations
- Universidad Peruana Cayetano Heredia
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Placebo Comparator
Experimental
Placebo Comparator
Experimental
CMS - placebo first
CMS - iron
SLR - placebo
SLR - iron
Patients with chronic mountain sickness (CMS) who are venesected and studied for several weeks. In the final crossover period of the study, patients receive a placebo (saline) infusion first followed by iron infusion.
Patients with chronic mountain sickness (CMS) who are venesected and studied for several weeks. In the final crossover period of the study, patients receive an iron infusion first followed by placebo (saline) infusion.
Sea level residents (SLR) taken to high altitude for one week, and receiving placebo (saline) infusion on Day 3 at high altitude.
Sea level residents (SLR) taken to high altitude for one week, and receiving iron infusion on Day 3 at high altitude.