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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RECRUITING
PHASE2
30 participants
INTERVENTIONAL
2026-01-26
2026-12-31
Brief Summary
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* Does the new contrast-free method provide more information about lung perfusion than SOC?
Participants will undergo a 30 minute chest CT.
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Detailed Description
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The primary objective of this study is to collect dynamic CT scan data with human participants using high frame rate imaging methods to produce a map of lung perfusion.
Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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CT scan
Participants undergoing a CT
CT scan
Dynamic contrast-free chest CT scan
Interventions
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CT scan
Dynamic contrast-free chest CT scan
Eligibility Criteria
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Inclusion Criteria
* Able to sign and date the informed consent form
* Will undergo a clinically-indicated CT exam of the head, neck, chest, abdomen, pelvis, or extremities
Exclusion Criteria
* In need of urgent or emergent care
* Have any conditions that, in the opinion of the PI or designee, would interfere with the evaluation of the results or constitute a health hazard for the participant
18 Years
ALL
No
Sponsors
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University of Wisconsin, Madison
OTHER
Responsible Party
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Principal Investigators
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Matthew Smith, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Wisconsin, Madison
Locations
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University of Wisconsin - Madison
Madison, Wisconsin, United States
Countries
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Central Contacts
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Other Identifiers
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SMPH/RADIOLOGY/RADIOLOGY
Identifier Type: OTHER
Identifier Source: secondary_id
AS
Identifier Type: OTHER
Identifier Source: secondary_id
Protocol Version 1/18/2025
Identifier Type: OTHER
Identifier Source: secondary_id
2025-0586
Identifier Type: -
Identifier Source: org_study_id
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