Reduction of Staph Aureus Carriage by Non-Antibiotic NOZIN® Nasal Sanitizer® Antiseptic
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| ClinicalTrials.gov Identifier: NCT01861457 |
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Recruitment Status :
Completed
First Posted : May 23, 2013
Results First Posted : April 22, 2015
Last Update Posted : April 22, 2015
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Infectious Disease | Other: Nozin® Nasal Sanitizer® Other: Placebo | Not Applicable |
The purpose of the proposed pilot study is to employ a repeated sampling protocol to test the effectiveness of a currently marketed, over-the-counter topical preparation to reduce carriage of Staphylococcus aureus (S. aureus) in the nasal vestibules of health professionals working in an outpatient clinical setting. The product to be tested is the NOZIN® Nasal Sanitizer® antiseptic produced by Global Life Technologies Corp. It is an alcohol-based, non-antibiotic antiseptic preparationl
The study has one primary Specific Aim:
To determine the extent to which colonization of the vestibular region of the nares by S. aureus can be reduced by a regimen of nasal topical applications of the alcohol-based antiseptic during the course of typical 10-hour work day in subjects known to exhibit S. aureus nasal carriage.
A secondary aim of the study will be to evaluate the concurrent effectiveness of the antiseptic applications on a measure of general bacterial colonization within the vestibules of each subject.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 39 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Investigator) |
| Primary Purpose: | Prevention |
| Official Title: | Reduction of Staph Aureus Carriage by Non-Antibiotic NOZIN® Nasal Sanitizer® |
| Study Start Date : | January 2013 |
| Actual Primary Completion Date : | April 2013 |
| Actual Study Completion Date : | May 2013 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Nozin® Nasal Sanitizer®
Non-antibiotic, alcohol-based antiseptic
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Other: Nozin® Nasal Sanitizer®
The treatment agent tested was the alcohol and natural oil preparation that comprises the commercially available over-the-counter (OTC) product, NOZIN® Nasal Sanitizer® antiseptic, by Global Life Technologies Corp, with the addition of benzalkonium chloride (0.13%), as described for the patented and safety-tested formulation.
Other Name: Nozin® Nasal Sanitizer® antiseptic |
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Placebo Comparator: Phosphate-buffered saline
Placebo
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Other: Placebo
The placebo preparation, utilized to account for the potential mechanical effects of the application process, was phosphate buffered saline (PBS).
Other Name: Sham |
- Treatment-associated Change in S. Aureus Colonization During a Typical 10-hour Work Day [ Time Frame: 10-hour work day ]The percent change from morning baseline sample to the evening sample taken at the end of a typical 10-hour workday in treated subjects known to be colonized by Staph aureus.
- Treatment-associated Change in Total Nasal Bacterial Colonization During a Typical 10-hour Work Day [ Time Frame: 10 hour workday ]The percent change from morning baseline sample to the evening sample taken at the end of a typical 10-hour workday in treated subjects known to be colonized by Staph aureus.
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| Ages Eligible for Study: | 18 Years to 70 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- All healthy health care professionals between the ages of 18 and 60 years of age who are regular full-time employees of the MUSC Hospital, work a 10 or 12 hour work shift, and test positive for nasal vestibular S. aureus carriage within 10 days prior to their scheduled study day will be eligible to participate in the study.
Exclusion Criteria:
- Excluded from the study will be individuals exhibiting symptoms of upper respiratory disease, including chronic rhinitis/sinusitis, seasonal allergies, upper respiratory infection during the previous four weeks, have known allergy to citrus or soy oil, or are "smokers". "Non-smokers" will be defined as those individuals who have abstained from smoking for at least one year prior to the study. Subjects must be able and agree to refrain from using prescription and non-prescription nasal spray or other nasal preparations or washes from the time of their screening up to and during their scheduled study day.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01861457
| United States, South Carolina | |
| Medical University of South Carolina | |
| Charleston, South Carolina, United States, 29425 | |
| Principal Investigator: | Shaun A Nguyen, MD | Medical University of South Carolina- Department of Otolaryngology - Head and Neck Surgery |
Publications of Results:
| Responsible Party: | Shaun A. Nguyen, Associate Professor- Department of Otolaryngology - Head and Neck Surgery, Medical University of South Carolina |
| ClinicalTrials.gov Identifier: | NCT01861457 |
| Other Study ID Numbers: |
Nozin |
| First Posted: | May 23, 2013 Key Record Dates |
| Results First Posted: | April 22, 2015 |
| Last Update Posted: | April 22, 2015 |
| Last Verified: | April 2015 |
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nasal sanitizer® S. aureus general bacteria nasal carriage decolonization |
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Communicable Diseases Infections Disease Attributes |
Pathologic Processes Anti-Infective Agents, Local Anti-Infective Agents |

