Oral Health
Conditions
Interventions
Sponsors
October 6 University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: I. Participants aged 18 years or above. II. Participants who will be able to provide written informed consent. III. Participants who will be confirmed as healthy by the examiner, without clinically significant diseases that can interfere with the study outcomes. IV. Participants with more than two sensitive teeth with dentin exposure due to gingival recession, abrasion, and erosion
Exclusion criteria
Exclusion criteria: I. Individuals who received treatment for dentin hypersensitivity within the past 4 weeks II. Individuals who had teeth with dentin hypersensitivity due to other reasons (e.g., dental caries and defective restorations) III. Individuals who had taken nonsteroidal anti-inflammatory drugs or narcotic analgesics within the past week IV. Individuals with clinically significant allergic diseases V. Pregnant or lactating women VI. Smokers VII. Individuals who used toothpaste specifically designed for treating dentin hypersensitivity in the past 4 weeks VIII. Individuals who may have undergone teeth bleaching treatment within the past 4 weeks IX. Individuals who underwent scaling or periodontal treatment within the past 4 weeks X. Individuals with teeth that had deep periodontal pockets (> 5 mm) XI. Individuals who underwent cervical restorative treatment (e.g., resin composite and glass ionomer)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain reduction | — |
Secondary
| Measure | Time frame |
|---|---|
| Dentin hypersensitivity | — |
Countries
Egypt
Contacts
Public ContactShereen Fahim
Associate Professor of Conservative Dentistry
Outcome results
None listed