"Solana™ Trichomonas Assay Field Study"

NCT02566447 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2018-03-20

No results posted yet for this study

Summary

The Solana® Trichomonas Assay is an in vitro qualitative nucleic acid amplification test for the detection of Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Helicase-Dependent Amplification (HDA) technology and the Solana instrument.

Conditions

  • Trichomonas Vaginalis

Interventions

DEVICE

Solana Trichomonas Assay Testing

Specimen collection of urine and/or vaginal swabs for testing

Sponsors & Collaborators

  • Quidel Corporation

    lead INDUSTRY

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-10-15
Primary Completion
2016-08-15
Completion
2016-08-15
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT02566447 on ClinicalTrials.gov