None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Individuals diagnosed with a score of DH higher than or equal to two in the verbal rating scale (VRS) after evaporative and tactile stimulation in one caries free molar tooth. Individuals older than 18 years and those who accepted to participate in the study after signing of the informed consent form.
Exclusion criteria
Exclusion criteria: Individuals who have undergone periodontal treatment or the treatment of DH within the last 30 days. Pregnant women. Individuals with decayed or filled teeth.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate and compare the effectiveness of Diode LASER therapy and dentin bonding agent in reducing dentin hypersensitivity in affected teeth.Timepoint: Baseline, immediatedly after procedure, 7 days, 30 days | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effectiveness of Diode LASER in reducing dentin hypersensitivity using a VAS and VRS scale. To evaluate the effectiveness of dentin bonding agent in reducing dentin hypersensitivity using a VAS and VRS scale. To compare the reduction in dentin hypersensitivity in LASER and Dentin bonding agent group. To compare and evaluate the decline in effectiveness of dentin bonding agent and Diode Laser in treating dentin hypersensitivity during a one-month period. Timepoint: Baseline, immediatedly after procedure, 7 days, 30 days | — |
Countries
India
Contacts
College of Dental Science and Hospital, Amargadh