NCT Number: NCT02225912
A Study to Evaluate the Efficacy of the Nasal Antiseptic, PrevinC, When Administered for the RiskReduction of Rhinitis in Subjects Who Work for Child Day Care Centers
The hypothesis was to establish whether the use of PrevinC administered nasally 2-3 times a day will prevent upper respiratory infections in otherwise healthy adults working in child day care centers.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Sunflower Preschool & Day Care, Hialeah, Florida, United States
Who can participate
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Subject must provide written informed consent prior to the conduct of any study
- Male or female
- 18-65 years of age
- Inclusive
- Employed by one of seven selected Day Care Centers
Exclusion criteria
- Recent symptoms of upper respiratory infection, respiratory disease
- Received medication for colds or allergies within 3 weeks of enrolling
- Had nasal surgery within 2 months of enrolling
- Had a pierced nose or wore nose jewelry
Treatment and study plan
Placebo
DrugPrimary outcomes
-
Rhinitis
Time frame: weekly from February 2005 to May 2005, up to 3 months
The incidence of rhinitis was measured on a weekly basis through evaluation of study diaries.
Sponsors and collaborators
Lead sponsor
BioHealth Technologies Inc.
Industry
Registry information
Important dates
- Study start
- 2005
- Primary completion
- 2005
- Study completion
- 2005
- First posted
- Aug 26, 2014
- Registry last updated
- Jan 16, 2019
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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