Clinical Performance of the Diassess Influenza A and B Test

NCT03035396 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 567

Last updated 2018-02-06

No results posted yet for this study

Summary

The primary objective of this study is device feasibility of the Diassess Influenza A and B Test

Conditions

Interventions

DEVICE

Diassess Influenza A and B Test

Sponsors & Collaborators

  • Diassess Inc.

    lead INDUSTRY

Principal Investigators

  • Carol Chen, PhD · Diassess Inc.

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-29
Primary Completion
2017-05-31
Completion
2017-05-31

Countries

  • United States

Study Locations

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Entities

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 NCT03035396 on ClinicalTrials.gov