Healthy dentate adult volunteers aged 18 or over Oral Health
Conditions
Interventions
This is an observational study. The clinical examination will involve capturing scores for the cervical localisation code on all eligible tooth surfaces, 7-7 both arches (buccal and palatal/lingual).
Sponsors
University of Bristol
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Healthy participants of either gender 2. Aged 18 or over 3. Understand and are willing, able and likely to comply with all study procedures and restrictions 4. Accept the form of the study and signs a declaration of informed consent 5. Have a minimum of 10 teeth not including implants or teeth with crowns and bridges
Exclusion criteria
Exclusion criteria: 1. An employee and/or family relative of the investigator dentist 2. Anyone who the investigator's opinion is not suitable to take part in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Inter- and Intra-examiner agreement of the proposed clinical classification (as assessed by the cervical localisation score) of the cervical region using three independent dentists assessing the same participants, in a randomised treatment sequence, at a single timepoint | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
England, United Kingdom
Outcome results
None listed