Health Condition 1: K038- Other specified diseases of hard tissues of teeth
Conditions
Interventions
None listed
Sponsors
DRKARANDE RUTVI
Eligibility
Inclusion criteria
Inclusion criteria: Patients between 18 to 60 years of age will be included. Patients showing good health, no history of allergies to dental products and medications, and adequate oral hygiene without active periodontal disease will be included in the study. Patients with atleast Non carious cervical lesions will be included ,regardless of their location in the arch. Teeth with NCCL depth equal to or greater than 1 mm and a maximum depth of 4 mm, with at least 50% of their margins devoid of enamel will be selected for the procedures. A millimetre probe will be used to measure the height, width, and depth of cavities in millimetres. Careful clinical examination, including pulpal vitality tests (sensitivity to cold, hot and percussion) will be verified by the absence of periapical alterations in the selected teeth. No attempt will be made to determine the etiology of the cervical lesions. A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.
Exclusion criteria
Exclusion criteria: Patients with smoking habit, poor oral hygiene, severe periodontal disease, mal-aligned and heavy bruxism resulting in lost physiologic contour will be excluded. Tooth indicated as an abutment for fixed partial denture and tooth having more than grade 1 mobility will be excluded Teeth with developmental anomaly or pathology or congenital defects will be excluded. Patients with previous cervical restorative procedure or caries lesions will be excluded. Pregnant or lactating women, individuals with active carious lesions, users of desensitizing agents, fluorine or orthodontic appliances, or with wear more than 50% wear will be excluded. Lesions involving cementum will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the effect of selective etch technique to extract of Emblica officinalis Epigallactocatechin-3-gallate and chlorhexidine on clinical performance of composite resin restoration in cases of NCCL using Revised FDI criteria at baseline, 6 months and 12 months.Timepoint: At baseline, 6 months and 12 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| nilTimepoint: nil | — |
Countries
India
Contacts
Public ContactDR DEEBAH CHOUDHARY
K.M.Shah Dental College And Hospital
Outcome results
None listed