Skip to main content
Clinical Trials/CTRI/2018/04/013038
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

Dabur India Limited0 sites139 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
October 15, 2013
Last Updated
4 years ago
Study Type
Interventional

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

Similar Trials