CTRI/2022/03/041320已完成未知
An Open Label, Single Arm, Clinical Study To Evaluate Efficacy And Safety Of A Sensitive Tooth Paste For Dentinal Hypersensitivity, Oral Hygiene And Dental Care.
Patanjali Ayurved Ltd0 个研究点目标入组 35 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 35
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Age:18 to 60 years (both inclusive) at the time of consent.
- •2.Sex:Healthy Male or non-pregnant/non-lactating female.
- •3.Females of Childbearing potential must have a negative urine pregnancy test performed during screening.
- •4.Subjects are in good general health as determined by the Investigator based on medical history and vital signs.
- •5.Subjects with no dental condition (Normal Group).
- •6.Subjects with mild, moderate and severe dental hypersensitivity (1:1:1).
- •7.Subjects with mild, moderate or severe plaque with plaque index of 2, 3 and 4.
- •8.Subjects with gingivitis and having extrinsic dental stains.
- •9.Subjects having T-VSC reading (total volatile sulphur compounds) of ââ?°Â¥140 ppb (parts per billion).
- •10.Subjects should be willing to come to the test site without brushing their teeth in the morning of screening visits.
- •11.Subjects should be willing to not consume anything except water after meal of previous night.
- •12.Subject must be able to understand and provide written informed consent to participate in the study.
- •13.Subjects willing and able to follow the study protocol and study directions, to participate in the study.
排除标准
- •1.Subject with orthodontic bands.
- •2.Subjects with plaque index of 0, 1 and 5.
- •3.Subject with partial removable dentures.
- •4.Subject having tumor (s) of the soft or hard tissues of the oral cavity.
- •5.Subject with advanced periodontal disease (purulent exudate, tooth mobility, and/or extensive loss of periodontal attachment or alveolar bone).
- •6.Subject with five or more carious lesions requiring immediate restorative treatment.
- •7.Subject having used antibiotic any time during the one month prior to entry into the study.
- •8.Subject having participation in any other dental clinical study within last six months prior to entry into the study.
- •9.Subjects with dental prophylaxis during the last two weeks prior to baseline examinations.
- •10. Subject with history of allergies to oral care/personal care consumer products or their ingredients.
- •11.Subjects on any prescription medicines that might interfere with the study outcome.
- •12.Subjects taking oral contraceptives and other medication-based contraceptives.
- •13.Female subjects who are pregnant or who are on lactation.
- •14.Consumption of any medicated sweets, chewing gum, breath fresheners, etc. containing anti-microbial agents.
- •15.Subjects with diseases or having history that potentially can contribute to oral malodor (e.g., diabetes mellitus, bronchitis, tonsillitis, sinusitis etc.)
- •16.Subjects who consume alcohol.
- •17.Subject smoking cigarette or consume any other form of tobacco.
研究者
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