Post-operative sensitivity in non carious cervical lesions using Universal adhesives
Phase 2
- Conditions
- Health Condition 1: K031- Abrasion of teethHealth Condition 2: K031- Abrasion of teeth
- Registration Number
- CTRI/2021/11/038198
- Lead Sponsor
- Saveetha Dental College and Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients 30-50 years of age
atleast 2 NCCLs in each quadrant
depth of the lesion 1-3mm,
presence of antagonist teeth.
Exclusion Criteria
poor gingival and periodontal health; uncontrolled rampant caries; bruxism; patients with systemic diseases.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduced VAS score for assessment of postoperative sensitivity at 24 hrs, 1week, 2weeks, 4 weeks.Timepoint: 24 hrs, 1week, 2weeks, 4 weeks.
- Secondary Outcome Measures
Name Time Method nilTimepoint: nil