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临床试验/NCT06300905
NCT06300905已完成3 期

Clinical Investigation on Oral Malodor for a New Formula of Stannous Toothpaste as Compared to Colgate Cavity Protection Toothpaste Using Organoleptic Method

Colgate Palmolive1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
100
试验地点
1
主要终点
Organoleptic Oral Malodor Evaluations

研究概览

简要总结

This 3-week clinical study was designed to investigate the clinical efficacy on oral malodor of a 0.454% stannous fluoride toothpaste with nitrate and pyrophosphate (referred to as SNAP) compared to Colgate Cavity Protection Toothpaste containing 0.76% sodium monofluorophosphate 12 hours post-brushing after 3 weeks of product use.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Must be male or female 18 to 70 years of age
  • Must be in good general health
  • Must be in good oral health based on self-assessment
  • Must be available during the weeks of this study for all appointment time points
  • Should have a minimum of 20 natural uncrowned teeth (excluding third molars)
  • Should have a baseline mean oral malodor score greater than or equal to 6.0 and less than or equal to 8.0
  • Must give written informed consent
  • No known history of allergy to personal care/consumer products or their ingredients

排除标准

  • Participation in any other oral clinical studies for the duration of this study
  • Full or partial (upper or lower) dentures
  • Pregnant or lactating (breast feeding)
  • Use of tobacco products
  • History of allergy to common toothpaste ingredients
  • Use of phenolic flavored products, such as mint flavored candies and chewing gum, the morning of the study and during the sampling periods
  • Immune compromised individuals (HIV, AIDS, immuno suppressive drug therapy)
  • Individuals who, due to medical conditions, cannot go without eating or drinking for the post use treatment evaluation time points (6 hrs. + overnight)

研究组 & 干预措施

Group I

Experimental

Brushing twice daily in the morning and evening with 2 minutes each time

干预措施: test product (Drug)

Group I

Experimental

Brushing twice daily in the morning and evening with 2 minutes each time

干预措施: Control product (Drug)

Group II

Active Comparator

Brushing twice daily in the morning and evening with 2 minutes each time

干预措施: test product (Drug)

Group II

Active Comparator

Brushing twice daily in the morning and evening with 2 minutes each time

干预措施: Control product (Drug)

结局指标

主要结局

Organoleptic Oral Malodor Evaluations

时间窗: Oral malodor evaluations at baseline & 3 weeks

The measured levels of oral malodor will be expressed in organoleptic scales (1-9)

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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