Community Acquired Pneumonia in Older Adults

NCT04709978 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2023-11-15

No results posted yet for this study

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

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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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04709978 on ClinicalTrials.gov