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Trial record 42 of 287 for:    Cerebral Hypoxia

Neuroimaging During Pure Oxygen Breathing

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ClinicalTrials.gov Identifier: NCT03268590
Recruitment Status : Completed
First Posted : August 31, 2017
Last Update Posted : July 24, 2018
Sponsor:
Information provided by (Responsible Party):
Michael J. Decker, Case Western Reserve University

Brief Summary:

The investigators will conduct a non-randomized clinical trial to examine the effect of pure oxygen breathing on the brain. The study will compare cerebral blood flow, cortical electrical activity, and cognitive performance in 32 persons during room air (21% oxygen) breathing and pure oxygen (100% oxygen) breathing. Subjects will be used as their own controls. The investigators aim to:

  1. Determine whether breathing 100% oxygen changes blood flow through the brain. The investigators will learn whether brain blood flow is increased, decreased or stays the same.
  2. Determine if changes that might occur in brain blood flow are also accompanied by changes in the brain's electrical activity (EEG).
  3. Learn whether changes in the speed at which the brain processes information (cognitive function) accompany changes in brain blood flow and electrical activity that may be seen.

Condition or disease Intervention/treatment Phase
Hyperoxia Hypoxia, Brain Neurobehavioral Manifestations Drug: Oxygen Phase 4

Detailed Description:
The investigators will conduct a two-arm crossover design clinical trial to compare the effect of room air breathing (21% inspired oxygen) with pure oxygen breathing (100% inspired oxygen) on brain blood flow and cortical electrical activity. The study involves a one-time data collection taking place at University Hospitals Cleveland Medical Center on the Case Western Reserve University campus in Cleveland, OH. The investigators will perform neuroimaging (MRI) with electroencephalographic (EEG) cortical network mapping and cognitive assessments in all participants during room air breathing and again while breathing 100% pure oxygen. Oxygen will be delivered through a non-rebreather mask. Arterial blood partial pressure of oxygen (PaO2) will be measured twice, from arterial blood samples drawn during breathing room air prior to the MRI scan and again after 30 minutes of breathing 100% oxygen immediately following neuroimaging. Thus, the investigators will be able to determine if breathing pure oxygen may temporarily change brain blood flow and breathing, leading to changes in cognitive status such as euphoria or slowed reflexes. Information gained in this study may have direct operational relevance by helping us to understand one potential cause of "Unexplained Physiologic Events" that are reported in some aircraft pilots when flying at high altitude. Information gained could lead to development of new gas mixtures for use by personnel working in low oxygen high altitude environments.

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 32 participants
Allocation: Non-Randomized
Intervention Model: Crossover Assignment
Intervention Model Description: Participants will undergo neuroimaging (MRI) with electroencephalographic (EEG) cortical network mapping and cognitive assessments during room air breathing (placebo). Room air (21% inspired oxygen) will be delivered via non-rebreather face mask. Persons will serve as their own control and undergo neuroimaging (MRI) with electroencephalographic (EEG) cortical network mapping and cognitive assessments during pure oxygen breathing. Pure oxygen (100% inspired oxygen) will be delivered via non-rebreather face mask
Masking: Double (Participant, Outcomes Assessor)
Primary Purpose: Basic Science
Official Title: Hyperoxia: An Unrecognized Mechanism for Inducing "Hypoxia-Like" Symptoms
Actual Study Start Date : October 2, 2017
Actual Primary Completion Date : May 2, 2018
Actual Study Completion Date : May 2, 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Oxygen Therapy

Arm Intervention/treatment
Sham Comparator: Room Air Breathing
Breathing 21% oxygen via non-rebreather face mask
Drug: Oxygen
Persons will undergo MRI, EEG, and complete computerized cognitive testing in baseline room air. Persons will then breathe 100% pure oxygen and undergo MRI, EEG, and complete computerized cognitive testing. Persons will serve as their own controls.

Active Comparator: Pure Oxygen Breathing
Breathing 100% oxygen via non-rebreather face mask
Drug: Oxygen
Persons will undergo MRI, EEG, and complete computerized cognitive testing in baseline room air. Persons will then breathe 100% pure oxygen and undergo MRI, EEG, and complete computerized cognitive testing. Persons will serve as their own controls.




Primary Outcome Measures :
  1. Cerebral Blood Flow [ Time Frame: At 30 minutes ]
    Change in brain blood flow from Baseline Room Air breathing (21% inspired oxygen) to Pure Oxygen breathing (100% inspired oxygen). Measured using Magnetic Resonance Imaging.


Secondary Outcome Measures :
  1. Cortical Network Activity [ Time Frame: At 30 minutes ]
    Change in cortical electrical activity from Baseline Room Air breathing (21% inspired oxygen) to Pure Oxygen breathing (100% inspired oxygen). Measured using MRI-compatible 64-electrode high-density electroencephalography (EEG).

  2. Cognitive Performance [ Time Frame: At 30 minutes ]
    Change in cognitive performance from Baseline Room Air breathing (21% inspired oxygen) to Pure Oxygen breathing (100% inspired oxygen). Measured using MicroCog Assessment of Cognitive Function.



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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Persons recruited from currently approved Human Subject Panel for high altitude studies at Wright Patterson Air Force Base, Dayton, OH. Volunteers will have documentation of past exposure to hypobaric conditions, either from past high-altitude flight, as hypobaric chamber personnel, or as participants in previous/current high altitude studies
  2. Height 152.5-195.5 cm, weight 40-135 kg.

Exclusion Criteria:

  1. Persons who have contraindications to MRI such as cardiac pacemakers, intracranial aneurysm clips, metallic implants or external clips within 10 mm of the head; implanted metallic devices such as pumps or previously implanted neurostimulation devices; cochlear implants, defibrillators, pacing wires, body piercings that cannot be removed, metal filings such as shrapnel, tattoos on the head and neck, or medical conditions contraindicated for MRI safety.
  2. History of claustrophobia

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03268590


Locations
United States, Ohio
Case Western Reserve University
Cleveland, Ohio, United States, 44106
Sponsors and Collaborators
Case Western Reserve University
Investigators
Principal Investigator: Michael J Decker, PhD Case Western Reserve University

Publications:

Responsible Party: Michael J. Decker, Associate Professor, Case Western Reserve University
ClinicalTrials.gov Identifier: NCT03268590     History of Changes
Other Study ID Numbers: CON215044
FA8650-12-D6280 TO0052 ( Other Grant/Funding Number: KBRWyle (for Wright Patterson AFB) )
First Posted: August 31, 2017    Key Record Dates
Last Update Posted: July 24, 2018
Last Verified: July 2018

Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Michael J. Decker, Case Western Reserve University:
Hyperoxia
Hypoxia, Brain

Additional relevant MeSH terms:
Hypoxia
Hyperoxia
Neurobehavioral Manifestations
Hypoxia, Brain
Signs and Symptoms, Respiratory
Signs and Symptoms
Neurologic Manifestations
Nervous System Diseases
Brain Diseases
Central Nervous System Diseases