Effects of Oxygen Status on Hypoxia Inducible Factor 1-α and Inflammation. A Pilot Proof of Principle Study.
NCT ID: NCT01889823
Last Updated: 2015-03-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
20 participants
INTERVENTIONAL
2013-06-30
2014-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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Hypoxia
Subjects will be breathing an individualized mix of nitrogen and room air titrated to an oxygen saturation of 80-85%.
Hypoxia
Subjects will be breathing an individualized mix of nitrogen and room air titrated to an oxygen saturation of 80-85%.
Hyperoxia
Subjects will be breathing 100% of oxygen
Hyperoxia
Subjects will be breathing 100% oxygen
Interventions
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Hypoxia
Subjects will be breathing an individualized mix of nitrogen and room air titrated to an oxygen saturation of 80-85%.
Hyperoxia
Subjects will be breathing 100% oxygen
Eligibility Criteria
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Inclusion Criteria
* Male
* Healthy
Exclusion Criteria
* Smoking
* History, signs or symptoms of cardiovascular disease
* History of atrial or ventricular arrhythmia
* (Family) history of myocardial infarction or stroke under the age of 65 years
* Cardiac conduction abnormalities on the ECG consisting of a 2nd degree atrioventricular block or a complex bundle branch block
* Hypertension (defined as RR systolic \> 160 or RR diastolic \> 90 mmHg)
* Hypotension (defined as RR systolic \< 100 or RR diastolic \< 50 mmHg)
* Renal impairment (defined as plasma creatinine \>120 μmol/l)
* Liver enzyme abnormalities alkaline phosphatase\>230 U/L and/or ALT\>90 U/L
* Medical history of any obvious disease associated with immune deficiency
* CRP \> 20 mg/L, WBC \> 12x109/L, or clinically significant acute illness, including infections, within 4 weeks before endotoxemia day
* Participation in a drug trial or donation of blood 3 months prior to the experiment
* Pre-existent lung disease or asthma
* Use of recreational drugs within 21 days prior to experiment day
* Visit to altitude \>1500m within 4 weeks prior to the experiment
* Air travel with flight time over 3 hours within 4 weeks prior to the experiment
* History of acute mountain sickness
* Recent hospital admission or surgery with general anaesthesia (\<3 months)
* Claustrophobia
* Feelings of discomfort during a 10 minute test wearing the transparent respiratory helmet at the screening visit
18 Years
35 Years
MALE
Yes
Sponsors
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Radboud University Medical Center
OTHER
Responsible Party
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Peter Pickkers
Prof. dr. P. Pickkers
Principal Investigators
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Dorien Kiers, MD
Role: PRINCIPAL_INVESTIGATOR
Intensive Care Medicine, Radboud University Nijmegen Medical Centre
Peter Pickkers, MD,PhD
Role: STUDY_DIRECTOR
Intensive Care Medicine, Radboud University Nijmegen Medical Centre
Locations
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Intensive Care Medicine, Radboud University Nijmegen Medical Centre
Nijmegen, Nijmegen, Gelderland, Netherlands
Countries
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Other Identifiers
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OX1
Identifier Type: -
Identifier Source: org_study_id
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