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临床试验/NCT07698938
NCT07698938已完成不适用

The Safety and Microbial Changes in the Use of Intranasal Neosporin®: A Prospective Study

Hospital Universitario Dr. Jose E. Gonzalez1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2025年2月13日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
12
试验地点
1
主要终点
Adverse events of intranasal Neosporin® in healthy participants.

研究概览

简要总结

Neosporin is an over-the-counter, FDA-approved triple-antibiotic ointment. It is widely used to treat and prevent skin infections following minor burns and injuries. Although the Neosporin® prospect indicates its use is strictly topical, it is often used intranasally by ear, nose, and throat specialists, plastic surgeons, and intensivists to prevent and treat various conditions. Nonetheless, no literature has documented the safety of intranasal Neosporin®. We designed a prospective study to assess the safety of this intervention in healthy participants and to investigate microbial changes before and after the intervention. Healthy participants will apply Neosporin® intranasally for 15 days and record daily adverse events and their severity. Nasal cultures will be drawn before and after the intervention and compared.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 65 years
  • Signed informed consent
  • Healthy volunteers

排除标准

  • Chronic or recurrent nasal conditions
  • Current use of other intranasal medications
  • History of severe allergic reactions to antibiotics
  • History of allergy to the components of Neosporin®
  • Participation in another research protocol
  • Being a staff member or an immediate family member of a staff member
  • Pregnant women

研究组 & 干预措施

Polymyxin B Sulfate 500,000 IU, Bacitracin zinc 40,000 IU, Neomycin Sulfate 0.35g neomycin base

Experimental

0.5 gr of Polymyxin B Sulfate 500,000 IU, Bacitracin zinc 40,000 IU, Neomycin Sulfate 0.35g neomycin base will be applied intranasally in healthy participants for 15 days

干预措施: Intranasal application of Polymyxin B Sulfate 500,000 IU, Bacitracin zinc 40,000 IU, Neomycin Sulfate 0.35g neomycin base (Drug)

结局指标

主要结局

Adverse events of intranasal Neosporin® in healthy participants.

时间窗: 16 days

次要结局

未报告次要终点

研究者

发起方
Hospital Universitario Dr. Jose E. Gonzalez
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Adrian Camacho-Ortiz

Head of Department

Hospital Universitario Dr. Jose E. Gonzalez

研究点 (1)

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