Community Acquired Pneumonia in Older Adults
NCT04709978 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75
Last updated 2023-11-15
Summary
This study will utilize diagnostic imaging and salivary biomarkers to estimate the prevalence of aspiration in older adults with suspected community-acquired bacterial pneumonia (CABP). 150 participants over the age of 60 diagnosed with pneumonia will be recruited into this study. 62 of these participants will be enrolled in a supplemental study.
Conditions
- Pneumonia
- Aspiration Pneumonia
Interventions
- DIAGNOSTIC_TEST
-
Videofluoroscopic Swallowing Study
Participants enrolled in supplemental study will swallow different barium containing liquid and food boluses types that are captured on fluoroscopic imaging in real time.
- DIAGNOSTIC_TEST
-
Nuclear medicine pulmonary aspiration study
Participants enrolled in supplemental study will be administered radiotracer (Tc-99m-Sulfur Colloid) orally and static images of the chest will then be obtained at specified intervals over the next 2 hours to determine location of the radiotracer.
- DIAGNOSTIC_TEST
-
TOR-BSST and 3 oz Water Swallow
The research specialist will conduct ten 1 tsp water swallows, one cup sip of water and a 3 ounce water swallow test with the patient. After each swallow, the participant is asked to say "ah" so that their voice quality can be assessed.
- DIAGNOSTIC_TEST
-
Sputum Culture
Patients will have sputum collected during stay (ED participants only)
- DIAGNOSTIC_TEST
-
MeMed BV®
A blood test to help determine if the infection is viral or bacterial (ED participants only)
- DIAGNOSTIC_TEST
-
Lung Ultrasound
To image the lungs (ED participants only)
- DIAGNOSTIC_TEST
-
Respiratory Function Tests
To measure respiratory pressures.
Sponsors & Collaborators
-
Gordon and Betty Moore Foundation
collaborator OTHER -
University of Wisconsin, Madison
lead OTHER
Principal Investigators
-
Michael Pulia, MD, MS · University of Wisconsin, Madison
Eligibility
- Min Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-02-24
- Primary Completion
- 2023-07-02
- Completion
- 2023-07-02
- FDA Drug
- Yes
Countries
- United States
Study Locations
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