Ignite Creation Date:
2025-12-25 @ 3:47 AM
Ignite Modification Date:
2026-03-11 @ 9:10 PM
Study NCT ID:
NCT00952302
Status:
COMPLETED
Last Update Posted:
2009-08-06
First Post:
2009-08-04
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Study of the Effects of Iron Levels on the Lungs at High Altitude
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006976', 'term': 'Hypertension, Pulmonary'}, {'id': 'D000532', 'term': 'Altitude Sickness'}, {'id': 'D000860', 'term': 'Hypoxia'}], 'ancestors': [{'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D006973', 'term': 'Hypertension'}, {'id': 'D014652', 'term': 'Vascular Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}, {'id': 'D012120', 'term': 'Respiration Disorders'}, {'id': 'D012818', 'term': 'Signs and Symptoms, Respiratory'}, {'id': 'D012816', 'term': 'Signs and Symptoms'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000077605', 'term': 'Ferric Oxide, Saccharated'}, {'id': 'D000077330', 'term': 'Saline Solution'}, {'id': 'D018962', 'term': 'Phlebotomy'}], 'ancestors': [{'id': 'D005290', 'term': 'Ferric Compounds'}, {'id': 'D058085', 'term': 'Iron Compounds'}, {'id': 'D007287', 'term': 'Inorganic Chemicals'}, {'id': 'D005937', 'term': 'Glucaric Acid'}, {'id': 'D013400', 'term': 'Sugar Acids'}, {'id': 'D000144', 'term': 'Acids, Acyclic'}, {'id': 'D002264', 'term': 'Carboxylic Acids'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D006880', 'term': 'Hydroxy Acids'}, {'id': 'D002241', 'term': 'Carbohydrates'}, {'id': 'D000077324', 'term': 'Crystalloid Solutions'}, {'id': 'D007552', 'term': 'Isotonic Solutions'}, {'id': 'D012996', 'term': 'Solutions'}, {'id': 'D004364', 'term': 'Pharmaceutical Preparations'}, {'id': 'D001800', 'term': 'Blood Specimen Collection'}, {'id': 'D013048', 'term': 'Specimen Handling'}, {'id': 'D019411', 'term': 'Clinical Laboratory Techniques'}, {'id': 'D019937', 'term': 'Diagnostic Techniques and Procedures'}, {'id': 'D003933', 'term': 'Diagnosis'}, {'id': 'D011677', 'term': 'Punctures'}, {'id': 'D013812', 'term': 'Therapeutics'}, {'id': 'D013514', 'term': 'Surgical Procedures, Operative'}, {'id': 'D008919', 'term': 'Investigative Techniques'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'BASIC_SCIENCE', 'interventionModel': 'CROSSOVER'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 33}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2008-10'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2009-08', 'completionDateStruct': {'date': '2008-11', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2009-08-04', 'studyFirstSubmitDate': '2009-08-04', 'studyFirstSubmitQcDate': '2009-08-04', 'lastUpdatePostDateStruct': {'date': '2009-08-06', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2009-08-06', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2008-11', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Change in pulmonary artery systolic pressure', 'timeFrame': 'One week (SLR arm) and one month (CMS arm)'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['Hypoxia', 'Iron', 'Hypoxia-Inducible Factor 1', 'Chronic mountain sickness'], 'conditions': ['Pulmonary Hypertension', 'Mountain Sickness']}, 'referencesModule': {'references': [{'pmid': '19809026', 'type': 'DERIVED', 'citation': 'Smith TG, Talbot NP, Privat C, Rivera-Ch M, Nickol AH, Ratcliffe PJ, Dorrington KL, Leon-Velarde F, Robbins PA. Effects of iron supplementation and depletion on hypoxic pulmonary hypertension: two randomized controlled trials. JAMA. 2009 Oct 7;302(13):1444-50. doi: 10.1001/jama.2009.1404.'}]}, 'descriptionModule': {'briefSummary': '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.', 'detailedDescription': '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.\n\nHIF 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.\n\nThis 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.'}, 'eligibilityModule': {'sex': 'MALE', 'stdAges': ['ADULT'], 'maximumAge': '60 Years', 'minimumAge': '18 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'SLR ARM\n\nInclusion Criteria:\n\n* sea level natives of lowland ancestry\n* generally in good health\n* detectable tricuspid regurgitation on echocardiography\n\nExclusion Criteria:\n\n* any significant medical problem\n* known susceptibility to high altitude pulmonary or cerebral oedema\n* taking medications or iron supplements\n\nCMS ARM\n\nInclusion Criteria:\n\n* diagnosis of chronic mountain sickness\n* no recent venesection therapy (within 1 year)\n* detectable tricuspid regurgitation on echocardiography\n\nExclusion Criteria:\n\n* any other significant medical problem'}, 'identificationModule': {'nctId': 'NCT00952302', 'briefTitle': 'Study of the Effects of Iron Levels on the Lungs at High Altitude', 'organization': {'class': 'OTHER', 'fullName': 'University of Oxford'}, 'officialTitle': 'Physiology Study Investigating the Effects of Supplementation and Depletion of Iron on Hypoxia-related Pulmonary Hypertension', 'orgStudyIdInfo': {'id': 'Oxford-Peru-2008'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'PLACEBO_COMPARATOR', 'label': 'CMS - placebo first', 'description': '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.', 'interventionNames': ['Procedure: Venesection', 'Drug: Iron sucrose', 'Drug: Normal saline']}, {'type': 'EXPERIMENTAL', 'label': 'CMS - iron', 'description': '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.', 'interventionNames': ['Procedure: Venesection', 'Drug: Iron sucrose', 'Drug: Normal saline']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'SLR - placebo', 'description': 'Sea level residents (SLR) taken to high altitude for one week, and receiving placebo (saline) infusion on Day 3 at high altitude.', 'interventionNames': ['Drug: Normal saline']}, {'type': 'EXPERIMENTAL', 'label': 'SLR - iron', 'description': 'Sea level residents (SLR) taken to high altitude for one week, and receiving iron infusion on Day 3 at high altitude.', 'interventionNames': ['Drug: Iron sucrose']}], 'interventions': [{'name': 'Iron sucrose', 'type': 'DRUG', 'otherNames': ['Venofer'], 'description': 'Single intravenous infusion of iron 200 mg', 'armGroupLabels': ['SLR - iron']}, {'name': 'Normal saline', 'type': 'DRUG', 'description': 'Single intravenous infusion of normal 0.9% saline 100 mls (as placebo)', 'armGroupLabels': ['SLR - placebo']}, {'name': 'Venesection', 'type': 'PROCEDURE', 'description': 'Isolvolaemic venesection of total 2 litres of blood - 500 mls each day for 4 days, replaced with normal saline.', 'armGroupLabels': ['CMS - iron', 'CMS - placebo first']}, {'name': 'Iron sucrose', 'type': 'DRUG', 'otherNames': ['Venofer'], 'description': 'Two intravenous infusions, each of 200 mg of iron, separated by one day.', 'armGroupLabels': ['CMS - iron', 'CMS - placebo first']}, {'name': 'Normal saline', 'type': 'DRUG', 'description': 'Two intravenous infusions of normal 0.9% saline 100 mls (as placebo), separated by one day.', 'armGroupLabels': ['CMS - iron', 'CMS - placebo first']}]}, 'contactsLocationsModule': {'locations': [{'zip': '31', 'city': 'Lima', 'country': 'Peru', 'facility': 'Universidad Peruana Cayetano Heredia', 'geoPoint': {'lat': -12.04318, 'lon': -77.02824}}], 'overallOfficials': [{'name': 'Peter A Robbins, BMBCh DPhil', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Oxford'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University of Oxford', 'class': 'OTHER'}, 'collaborators': [{'name': 'Universidad Peruana Cayetano Heredia', 'class': 'OTHER'}], 'responsibleParty': {'oldNameTitle': 'Ms Heather House, Head of Clinical Trials and Research Governance', 'oldOrganization': 'University of Oxford'}}}}