A Multi-Site Clinical Evaluation of the ARIES Clostridium Difficile Assay in Symptomatic Patients

NCT02497417 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1021

Last updated 2017-08-23

No results posted yet for this study

Summary

The ARIES C. difficile Assay is a real-time PCR based qualitative in vitro diagnostic test for the direct detection of C. difficile nucleic acid in stool specimens.

Conditions

Sponsors & Collaborators

  • Luminex Corporation

    lead INDUSTRY

Principal Investigators

  • Ronald Dunn · Luminex Corporation

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-31
Primary Completion
2017-02-28
Completion
2017-02-28

Countries

  • United States

Study Locations

More Related Trials

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 NCT02497417 on ClinicalTrials.gov