None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)patients with good health in the range of 18-50 years. 2)patients with minimum of two hypersensitive teeth which are anterior to the molars and demonstrated cervical abrasion or gingival recession. 3)defects less than 1mm loss of tooth structure in depth which doesnot require restorative treatment. 4)patients were required to be available during the duration of the study and to sign an informed consent form.
Exclusion criteria
Exclusion criteria: 1)patients using any desensitising agent 3 months before the participation in this study. 2)patients with a history of any systemic illness such as diabetes, hypertension or any form of medication such as anti-inflammatory, analgesics, or antibiotics. 3)patients with underlying gross pathologies. 4)pregnant and lactating females were excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of instant relief from symptoms of dentinal hypersensitivityTimepoint: Assessed immediately and post application after 1,2,4 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of RemineralisationTimepoint: Assessed immediately and post application after 1,2,4 weeks | — |
Countries
India
Contacts
Lenora Institute of Dental Sciences