Assessment of Assay for Rapid Identification of Bloodstream Infections From Whole Blood
NCT04147975 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 225
Last updated 2019-11-01
Summary
The purpose of this study is to assess the effectiveness of RaPID/BSI by testing its performance compared to blood cultures collected prospectively from consented subjects.
Conditions
- Bacteremia
- Candidemia
Interventions
- DIAGNOSTIC_TEST
-
RaPID/BSI Test
RaPID/BSI Test
Sponsors & Collaborators
-
HelixBind, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-10-01
- Primary Completion
- 2020-09-30
- Completion
- 2020-10-30
- FDA Device
- Yes
Countries
- United States
Study Locations
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