A clinical study for the comparison and evaluation of the role of three different agents in the treatment of dentinal hypersensitivity of teeth among the affected patients.
Phase 4
- Conditions
- Health Condition 1: K088- Other specified disorders of teethand supporting structures
- Registration Number
- CTRI/2024/05/066921
- Lead Sponsor
- Guru Nanak Institute of Dental Science and Researchri
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Systemically healthy patients with the chief complaint of dentinal hypersensitivity affecting a minimum of single tooth in the oral cavity.
2. Presence of gingival recession , attrition , abrasion , abfraction lesion.
3. No radiographic evidence of periapical lesions associated with the tooth.
Exclusion Criteria
1. Patients who have undergone professional desensitizing treatment or used desensitizing toothpaste for the last 3 months.
2.Presence of periodontal disease or undergoing treatment for the same.
3.Tooth affected by caries or irreversible pulpitis.
4. Tooth with cervical restoration or presence of full coverage crown .
5. Medically compromised patients.
6. Pregnant or lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The efficacy of the three different desensitizing agents for the treatment of dentinal hypersensitivity .Timepoint: Immediate post-operatively , after 7 days , after 14 days , after 1 month.
- Secondary Outcome Measures
Name Time Method Comparative evaluation of the clinical efficacy of the three different desensitizing agents in the management of dentinal hypersensitivityTimepoint: Immediate post-operatively , after 7 days , after 14 days , after 1 month