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NCT02979730: FluProcess

Impact of Rapid Flu Testing in BMC ED

Completed NA Last updated 24 July 2018
What this trial tests

NA trial testing Core Lab Test in Influenza-Like Illness in 233 participants. Completed in 1 December 2017.

Timeline
7 February 2017
Primary endpoint
1 December 2017
1 December 2017

Quick facts

Lead sponsorBoston Medical Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment233
Start date7 February 2017
Primary completion1 December 2017
Estimated completion1 December 2017
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Boston Medical Center

Who can join

21 and older, any sex, with Influenza-Like Illness or Influenza. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to compare Emergency Department patients who undergo influenza testing using an FDA-approved point-of-care device (Cobas Liat Influenza A/B assay) located in the ED, to patients whose samples are sent to the BMC central laboratory. Patients who agree to participate will have their samples randomly assigned to be tested on either at the core lab, or on the POC device. The current turnaround time for samples sent to the laboratory is approximately two hours; investigators expect that the point of care device can reduce this time. Investigators will determine if the time to disposition and the administration of antibiotics is different in the group undergoing POC influenza testing compared to those undergoing laboratory-based influenza testing

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Boston Medical Center trials

Trials by the same sponsor.

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