Not yet recruiting NCT07614685

Phase Resolved Functional Lung MRI and Oscillometry for the Observation of Healthy Lung Function

— Observational Breathing Lung Function Decreased MRI Imaging Healthy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Airway Oscillometer, Phase Resolved Functional Lung MRI.
Who it may be relevant to: Registry conditions: Breathing, Lung Function Decreased, MRI Imaging, Healthy. Basic parameters: from 18 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: United States
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Overview

This study will examine the relationship of airways resistance measured by oscillometry with ventilation defects measured by Phase Resolved Functional Lung (PREFUL) MRI in healthy human subjects.

Interventions

Device Airway Oscillometer
The termoflo c-100 Airwave Oscillometer System is intended to measure respiratory system impedance using the Forced Oscillation Technique (FOT).
Diagnostic test Phase Resolved Functional Lung MRI
The Phase Resolved Functional Lung (PREFUL) MRI technique acquires images of the lung so that measures of ventilatory defect percentage can be calculated.

Primary outcome measures

Oscillometer [Time frame: Single measurement, approximately 1 day]
Phase Resolved Functional Lung (PREFUL) MRI [Time frame: Single measurement, approximately 1 day]

Eligibility criteria

Inclusion criteria

Age 18 years or older
Ability to provide consent
Willingness to perform MRI and breathing test
Must be able to speak and understand English

Exclusion criteria

Pregnant
Unable or willing to provide consent or perform the required maneuvers for testing.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model: Cohort

Study locations

United States · 1 center

University of Rochester Medical Center — Rochester

Identifiers

NCT: NCT07614685 · STUDY00011843

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗