CTRI/2018/04/013038
Completed
Phase 2
A Clinical trial to evaluate the efficacy and comparison of a dentifrice containing Sodium Fluoride; 8% Strontium Acetate, Strontium Acetate (in Herbal Base) and two different Herbal dentifrices in reducing Dentinal Hypersensitivity
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: K038- Other specified diseases of hard tissues of teeth
- Sponsor
- Dabur India Limited
- Enrollment
- 139
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subjects with dental hypersensitivity complaints
Exclusion Criteria
- •1\. Subjects who had dental pathology causing pain similar to cervical dentinal hypersensitivity (such as teeth with caries, the presence of orthodontic appliances and restorations and/or the presence of a history of periodontal surgery in the area of the tooth during the previous three months)
- •2\. Subjects who had taken any medication
- •3\. Subjects who received professional treatment with desensitizing agents in the previous six months
- •4\. Subjects who received any treatment in the past 3 months
- •5\. Subjects who were pregnant or lactating
- •6\. Subjects who had any systemic diseases and/or the presence of a vital bleaching history
Outcomes
Primary Outcomes
Not specified
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