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Study done to check the efficacy of bonding material used for filling the tooth

Phase 2
Registration Number
CTRI/2018/08/015410
Lead Sponsor
Vokkaligara Sangha Dental College and hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patient requiring restoratons in the cervical region in a minimum of two sides and one tooth in each side

2. Cervical lesions with a depth of 1-3mm and width of 2-4mm

3. Patients willing to participate and sign the informed consent form

4. Subjects who have natural dentition directly opposing the test restoration.

•Patients having good oral hygiene

Exclusion Criteria

1.ndividual with a chronic systemic disease with or without oral manifestations.

2. Individual with periodontal problems.

3. Subjects with known allergy to any materials used

4. Individual with bruxism and other parafunctional habits

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Marginal staining <br/ ><br>Sensitivity <br/ ><br>FractureTimepoint: 7 days <br/ ><br>6months <br/ ><br>1 year
Secondary Outcome Measures
NameTimeMethod
Marginal staining <br/ ><br>Sensitivity <br/ ><br>FractureTimepoint: 7 days <br/ ><br>6months <br/ ><br>1 year
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