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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05462600
Other study ID # 801980
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date July 19, 2022
Est. completion date June 30, 2025

Study information

Verified date May 2023
Source University of California, San Diego
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Respiratory physiology involves a complex interplay of elements including control of breathing, respiratory drive, pulmonary mechanics, distribution of ventilation and gas exchange. Body position may also play an important role in respiratory mechanics. While effective methods exist for measuring these variables, they are typically measured in isolation rather than in combination. In pulmonary disease, decreasing mechanical stress and strain and optimizing transpulmonary pressure or the distending pressure across the lung, minimizing overdistention and collapse are central to clinical management. Obesity has a significant impact on pulmonary mechanics and is a risk factor for obstructive sleep apnea (OSA). However, our understanding of these elements is limited even in the general population. The investigators plan to use various validated methods to assess control of breathing, respiratory drive, distribution of ventilation and gas exchange to obtain a better understanding of underlying physiologic signatures in patients with and without obesity and the role of posture/position, with a secondary analysis comparing participants with and without obstructive sleep apnea.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 40
Est. completion date June 30, 2025
Est. primary completion date June 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 years or older - Non-smokers Exclusion Criteria: - <18 years old - 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

Study Design


Intervention

Other:
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).

Locations

Country Name City State
United States University of California San Diego Health La Jolla California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Diego

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Distribution of ventilation Change in regional ventilation distribution (ventral/dorsal) measured through electrical impedance tomography (EIT) 3 hours
Primary Respiratory drive Respiratory drive differences will be measured by mean desaturation (change from baseline percent oxygen saturation) following breath-hold maneuvers 3 hours
Primary Respiratory drive Respiratory drive differences will be assessed by the duration of maximal breath-hold (seconds) 3 hours
Primary Respiratory drive Respiratory drive will also be assessed by measurement of occlusion pressure (cm H2O) at 100 ms (P0.1) after the initiation of an inspiratory effort against a closed circuit. 3 hours
Secondary Pulmonary mechanics Pulmonary mechanics will be measured by transpulmonary pressure (cmH2O)obtained from esophageal manometry (transpulmonary pressure= airway pressure- esophageal pressure) 3 hours
Secondary Dead space fraction Dead space fraction will be calculated by partial pressure arterial/transcutaneous CO2 (PCO2) minus partial pressure of CO2 in mixed expired gas divided by the partial pressure of arterial/transcutaneous CO2 3 hours
Secondary Ventilatory ratio Ventilatory ratio will be calculated as measured minute ventilation multiplied by the measured partial pressure of PCO2 divided (transcutaneous) by the predicted minute ventilation based on ideal body weight multiplied by the ideal PaCO2 3 hours
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