None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Systemically healthy individuals both males and females;patients with at least 3 caries free cervical lesions with dentin hypersensitivity; Teeth which demonstrated erosion, abrasion or recession of gingiva less than 4mm; loss of dentin less than 2mm
Exclusion criteria
Exclusion criteria: Teeth with evidence of pulpitis, defective restoration, cracked enamel, active periodontal disease, active caries, deep cervical abrasion involving pulp; endodontically treated teeth; patients with history of drug addiction and use of analgesic and antiinflammatory drug;pregnant and lactating women; history of allergy and idiosyncratic reactions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To clinically evaluate and compare pain measurementTimepoint: 2 month | — |
Secondary
| Measure | Time frame |
|---|---|
| To clinically evaluate and compare the duration of action of two different desensitizing agentsTimepoint: 2 months | — |
Countries
India
Contacts
Jagadguru Shri Shivarathreeshwara University (JSS University)