Distribution of Ventilation, Respiratory Drive and Gas Exchange: Measurements and Monitoring
NCT ID: NCT05462600
Last Updated: 2025-04-11
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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ENROLLING_BY_INVITATION
40 participants
OBSERVATIONAL
2022-07-19
2026-12-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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BMI>24.9 kg/m2
Position change
Distribution of ventilation, respiratory drive, pulmonary mechanics and gas exchange will be measured in 3 unique positions: prone, head of bed (HOB) flat (i.e. 0 degrees) and HOB elevated (i.e. 30 degrees).
BMI 18-24.9 kg/m2
Position change
Distribution of ventilation, respiratory drive, pulmonary mechanics and gas exchange will be measured in 3 unique positions: prone, head of bed (HOB) flat (i.e. 0 degrees) and HOB elevated (i.e. 30 degrees).
Interventions
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Position change
Distribution of ventilation, respiratory drive, pulmonary mechanics and gas exchange will be measured in 3 unique positions: prone, head of bed (HOB) flat (i.e. 0 degrees) and HOB elevated (i.e. 30 degrees).
Eligibility Criteria
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Inclusion Criteria
* Non-smokers
Exclusion Criteria
* Significant history of pulmonary disease
* Chest wall, anatomical, physical abnormalities, skin integrity issues precluding placement of electrode belt in direct contact with skin
* Skin integrity issues precluding placement of nose clips, or transcutaneous carbon dioxide monitoring
* Inability to form a seal around a mouthpiece
* Known esophageal strictures, webs, or varices (if esophageal manometry to be included)
* Known platelet count \< 100,000 (if esophageal manometry to be included)
* On therapeutic anticoagulation (if esophageal manometry to be included)
* Known multidrug resistant (MDR) pulmonary infection
* Non-English language speakers
* Chronic hypoxemic respiratory failure
* Confirmed or suspected intracranial bleed, stroke, edema
* Active implants (i.e. implantable electronic devices such as pacemakers, cardioverter defibrillators or neurostimulators) or if device compatibility is in doubt
* Pregnant or lactating patients as safety and efficacy for use of EIT in such cases has not been verified
18 Years
ALL
Yes
Sponsors
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University of California, San Diego
OTHER
Responsible Party
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Alex Pearce
Principal Investigator
Principal Investigators
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Alex Pearce
Role: PRINCIPAL_INVESTIGATOR
University of California, San Diego
Locations
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University of California San Diego Health
La Jolla, California, United States
Countries
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Other Identifiers
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801980
Identifier Type: -
Identifier Source: org_study_id
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