Trials / Completed
CompletedNCT05937126
Rapid Diagnostic Supporting Antimicrobial Stewardship in Patients With Pneumonia
Rapid Diagnostic Supporting Antimicrobial Stewardship in Patients With Pneumonia (RASP) - A Quality Improvement Theragnostic Stewardship Project
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 1,203 (actual)
- Sponsor
- Mayo Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether or not the FilmArray Penumonia Panel adds value to patient care.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | FilmArray Pneumonia Panel | FDA-approved/cleared molecular, multiplex device that rapidly identifies viruses, bacteria, and antimicrobial resistance genes in sputum-like and bronchoalveolar lavage (BAL)-like specimens obtained from individuals with signs of a lower respiratory tract infection. |
| DIAGNOSTIC_TEST | Culture and antimicrobial susceptibility testing | Standard of care Gram stain, culture and other clinically ordered tests will be performed per standard practice. |
Timeline
- Start date
- 2020-09-15
- Primary completion
- 2022-09-19
- Completion
- 2022-09-19
- First posted
- 2023-07-10
- Last updated
- 2023-07-10
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05937126. Inclusion in this directory is not an endorsement.