Clinical Durability and Longevity of Cervical Composite restorations - A One Year follow-up Clinical study
Not Applicable
- Conditions
- Health Condition 1: K031- Abrasion of teeth
- Registration Number
- CTRI/2022/10/046298
- Lead Sponsor
- YASMEEN MOHAMMED AZEEM
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Volunteers with the presence of at least two non-carious cervical lesions, permanent dentition with age group of 18 ââ?¬â?? 65years, cervical margin in dentin, vital pulp with absence of symptoms of pulpitis such as spontaneous pain or sensitivity to pressure and with good oral hygiene.
Exclusion Criteria
Volunteers with severe periodontal disease, severe systemic diseases, allergy to any material used, very poor oral hygiene, pregnant or breast feeding, exposure to overload due to crowding of teeth and cervical carious lesions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome: Evaluation of longevity of restoration using FDI criteria <br/ ><br> <br/ ><br>Timepoint: Baseline, 3months, 6 months and 12 months <br/ ><br>
- Secondary Outcome Measures
Name Time Method Secondary outcome: Quality of life using OHIP 14 criteriaTimepoint: Baseline, 3months, 6 months and 12 months