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Assessment of Assay for Rapid Identification of Bloodstream Infections From Whole Blood

H

HelixBind

Status

Unknown

Conditions

Candidemia
Bacteremia

Treatments

Diagnostic Test: RaPID/BSI Test

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

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.

Enrollment

225 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Determined to have a positive blood culture.

Exclusion criteria

Trial design

225 participants in 1 patient group

Patients Suspected of Bloodstream Infection
Description:
No intervention(s) to be administered.
Treatment:
Diagnostic Test: RaPID/BSI Test

Trial contacts and locations

1

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Central trial contact

Michael Reeve

Data sourced from clinicaltrials.gov

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