CompletedNot applicableNCT02862262
A Multi-Site Clinical Evaluation of the ARIES Bordetella Assay in Symptomatic Patients
Studying Whooping cough
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Luminex Molecular Diagnostics
- Principal Investigator
- Ronald DunnLuminex Molecular Diagnostics
- Intervention
- ARIES Bordetella Assay(device)
- Enrollment
- 1052 enrolled
- Eligibility
- All sexes
- Timeline
- 2016 – 2016
Study locations (6)
- Indiana University Health, Indianapolis, Indiana, United States
- St. John Hospital and Medical Center, Grosse Pointe Woods, Michigan, United States
- Tricore, Albuquerque, New Mexico, United States
- Nationwide Children's Hospital Laboratory, Columbus, Ohio, United States
- Marshfield Labs, Marshfield, Wisconsin, United States
- Luminex Molecular Diagnostics, Toronto, Ontario, Canada
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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