Quantitative Pulmonary Imaging Registry & Biorepository
ConditionPulmonary Disease
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Kansas Medical Center
About this trial
The goal of this project is to establish a registry and biorepository of images and biological samples from subjects undergoing novel pulmonary imaging methods to be used for future research aimed toward identifying clinical applications of imaging methods and toward understanding the physiological significance of imaging biomarkers. This registry and biorepository will accelerate the development of these imaging techniques and may lead toward future clinical adoption of quantitative pulmonary imaging.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
The participant is enrolling/has enrolled in a research study at the University of Kansas Medical Center that involves Pulmonary MRI and/or Pulmonary CT.
Disqualifiers
The participant declines to participate.
Trial population
Participating in an Imaging Study at KUMC
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Collect Clinical Data
Collect relevant medical history (including demographic information, diagnoses, medical tests, smoking history), for patients participating in pulmonary imaging research.
Time frame
From Enrollment to 3 Months2
Establish a Biorepository
Establish a collection of biospecimens from imaging subjects to foster an improved understanding of the physiological significance of imaging biomarkers.
Time frame
From Enrollment to 3 Months3
Biospecimen Collection
Correlate imaging biomarkers with biospecimens and physiological/vital signs data.
Time frame
From Enrollment to 6 Months4
Collaborate
Provide images and biospecimens to researchers working to develop analysis methods for pulmonary CT and MRI. Separate IRB approval, alongside appropriate data and/or materials transfer agreements will be needed for these studies.
Time frame
From Enrollment to 12 MonthsSponsors and contacts
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Source ClinicalTrials.gov