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

Clinical efficacy of universal adhesive for the restoration of non carious cervical lesion:A Randomized clinical trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/08/015410

Enrollment

100

Registered

2018-08-23

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Self and Selective etching technique: To evaluate the bonding ability of self etch and selective etch technique for universal bonding agent used for restoring non carious cervical lesio

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
Marginal staining Sensitivity FractureTimepoint: 7 days 6months 1 year	—

Secondary

Measure	Time frame
Marginal staining Sensitivity FractureTimepoint: 7 days 6months 1 year	—

Countries

India

Contacts

Public ContactRanjitha G R

Vokkaligara Sangha Dental College

vikramgowda.dent@gmail.com9986379039

Outcome results