A clinical trail to study the effects of two sensitivity reducing agents in patients with sensitivity
- Conditions
- Health Condition 1: null- DENTINAL HYPERSENSITIVITYHealth Condition 2: K038- Other specified diseases of hard tissues of teeth
- Registration Number
- CTRI/2016/04/006882
- Lead Sponsor
- arayana Dental College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
1.Dentinal hypersensitivity caused by attrition, abrasion on any surface of tooth which do not need restorations.
2.Patients without any dental pathology which causes pain similar to dentinal hypersensitivity.
3.Pre-operative VAS score of morethan or equal to 2.
4.Patients in the age group of 18 to 50 years.
5.Patients with good systemic health.
1.Patients allergic to ingredients used in the study.
2.Teeth with caries, defective restorations, occlusal restorations, chipped teeth.
3.Teeth with deep periodontal pockets (probing depth >6 mm)
4.Patients with ulcerative gingivitis and stomatitis and those who have undergone periodontal surgery within the previous 3 months
5.Subjects with orthodontic appliances
6.Teeth with cervical defects >2mm horizontally
7.Patients who have used desensitizing toothpaste in the last 3 months.
8.Patients who were chronic use of anti-inflammatory andanalgesic medication.
9.Uncontrolled systemic diseases where oral hygiene is concerned.
10.Any gross oral pathology.
11.Uncontrolled systemic diseases where oral hygiene is concerned.
12.Patients who were pregnant or lactating.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method