Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
500 participants
OBSERVATIONAL
2007-02-28
2008-09-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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1
Patients with respiratory illnesses.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Illness onset within past 5 days
3. Symptoms of fever (\>=38°) plus one or more of the following: cough, runny nose, congestion, or sneezing (twice or more within one day). These symptoms must be present at the time of presentation to the emergency department (ED) or admission to the hospital.
4. Patient or parent/guardian is able to give informed consent
Exclusion Criteria
2. Participant/caregiver cannot be reached by phone in 7-10 days
3. Patient has a condition that can compromise respiratory function or the handling of respiratory secretions (e.g., severe cognitive dysfunction, spinal cord injuries, or other neuromuscular disorders)
30 Days
ALL
No
Sponsors
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National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Responsible Party
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Locations
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Children's Hospital Boston - Infectious Diseases
Boston, Massachusetts, United States
Beth Israel Deaconess Medical Center - Medicine - Infectious Disease
Boston, Massachusetts, United States
Countries
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Other Identifiers
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06-0096
Identifier Type: -
Identifier Source: org_study_id