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临床试验/NCT01345292
NCT01345292已完成不适用

Assessment of a Potassium Oxalate-Containing Formulation for the Relief of Dentinal Hypersensitivity

Johnson & Johnson Consumer and Personal Products Worldwide1 个研究点 分布在 1 个国家目标入组 226 人开始时间: 2011年4月最近更新:
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
入组人数
226
试验地点
1
主要终点
Mean Tactile Sensitivity Score at Week 2

研究概览

简要总结

This study is for people with sensitive teeth and involves going to the dentist for 4 visits over 6 weeks.

During the first 2 weeks, you will just brush your teeth two times a day with the fluoride toothpaste provided.

Then you will be assigned to a group if you qualify to continue in the study. All groups will get a marketed toothpaste and one group will also get a mouthwash with an experimental ingredient. You will have an equal chance of being assigned to any one of the three groups.

For the next 4 weeks, you will brush with your assigned toothpaste and rinse with your assigned mouthwash if assigned to the mouthwash group. A dentist will look at your mouth, teeth, tongue and gums and check for sensitive teeth. The investigators will see if the mouthwash helps to reduce tooth sensitivity during the study.

详细描述

This is an observer-blind, randomized, parallel-group, single-center, controlled clinical trial. Approximately 246 generally healthy adults meeting the necessary inclusion/exclusion criteria will be enrolled so that 210 subjects (70 per group) would reasonably be expected to complete the study. Subjects will have their oral soft/hard tissues assessed and will be evaluated for sensitivity levels at Screening (Visit 1), Baseline (Visit 2), Visit 3 at Week 2 and Visit 4 at Week 4. During the first two weeks of the study, subjects will be instructed to brush their teeth for one minute in their usual manner, twice daily, using the provided standard fluoride toothpaste. Subjects will return for the Baseline exam and, upon qualification with entry criteria, will be assigned to one of three treatment groups. Qualified subjects will be instructed to brush their teeth two times daily for one minute in their usual manner using the provided toothpaste (standard fluoride toothpaste or 5% potassium nitrate toothpaste). Subjects assigned to the mouthrinse group will be instructed to rinse twice daily, after brushing, with the provided mouthrinse for 60 seconds using 10 ml, for 4 consecutive weeks.

研究设计

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

入排标准

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

入选标准

  • Males and females at least 18 years of age in good general and oral health without any known allergy to commercial dental products or cosmetics.
  • Evidence of a personally signed and dated informed consent document indicating the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial.
  • Willingness to use the assigned products according to instructions, availability for appointments, and likelihood of completing the clinical trial.
  • The appropriate number and location of eligible teeth, based on protocol-defined standards.
  • Adequate oral hygiene (i.e., brush teeth daily and exhibit no signs of oral neglect).

排除标准

  • Any medical or dental history or condition, or use of any medication or drug, that per protocol or in the opinion of the investigator might compromise subject comfort or safety, or the analysis of study results.
  • Volunteers who have been using any of the following within protocol-defined timeframes:
  • home-care bleaching, whitening products or professional bleaching treatment
  • desensitizing agents whether prescribed or over-the-counter
  • sensitivity toothpastes, mouthwash or oral care products used for the treatment of dentinal hypersensitivity
  • Women who are pregnant, nursing or plan to become pregnant during the course of the study.

研究组 & 干预措施

12027-027

Experimental

Rinse with 10 ml of the assigned mouthwash for 60 seconds after you brush in your usual manner twice daily for one minute using at least a one-inch strip of the assigned toothpaste

干预措施: Mouthwash (Device)

310158077046

Active Comparator

Brush in your usual manner twice daily for at least one minute using at least a one-inch strip of the assigned toothpaste

干预措施: Potassium nitrate toothpaste (Drug)

037000003212

Placebo Comparator

Brush in your usual manner twice daily for at least one minute using at least a one-inch strip of the assigned toothpaste

干预措施: Sodium fluoride toothpaste (Drug)

结局指标

主要结局

Mean Tactile Sensitivity Score at Week 2

时间窗: 2 weeks

Tooth sensitivity was measured using a Yeaple probe. The force at which discomfort was felt by the participant was recorded on a scale of 10-80 grams. The score for each participant was calculated by averaging the scores for all study teeth for that participant.

Mean Tactile Sensitivity Score at Week 4

时间窗: 4 weeks

Tooth sensitivity was measured using a Yeaple probe. The force at which discomfort was felt by the participant was recorded on a scale of 10-80 grams. The score for each participant was calculated by averaging the scores for all study teeth for that participant.

次要结局

  • Mean Cold Air Stimulus VAS Score at Week 4(4 weeks)
  • Global Subjective VAS Score at Week 2(2 weeks)
  • Global Subjective VAS Score at Week 4(4 weeks)
  • Mean Cold Air Stimulus VAS Score at Week 2(2 weeks)
  • Mean Tactile Sensitivity Visual Analog Scale (VAS) Score at Week 2(2 weeks)
  • Mean Tactile Sensitivity VAS Score at Week 4(4 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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