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Tooth Wear Monitoring Using Intraoral Scanner

Tooth Wear Monitoring Using Intraoral Scanner. Identification of Etiological Factors and Patient Satisfaction.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05843513
Enrollment
46
Registered
2023-05-06
Start date
2019-01-18
Completion date
2021-08-30
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Wear

Keywords

Dental wear, Intraoral scanner, Etiological factors, Monitoring

Brief summary

The overall objective was to evaluate the monitoring of tooth wear using the intraoral scanner. Forty-six participants were selected according to the established inclusion and exclusion criteria. Monitoring of tooth wear, evaluation of possible aetiological factors, as well as patient satisfaction with the use of the intraoral scanner were carried out.

Detailed description

The overall objective was to evaluate the monitoring of tooth wear using the intraoral scanner. The specific objectives were (1) to determine whether the intraoral scanner is capable of detecting tooth wear superior to traditional visual indices, (2) to identify whether any aetiological factors may be associated with tooth tissue loss, (3) to establish a degree of patient satisfaction with the intraoral scanner as a diagnostic tool. Forty-six participants were selected according to the established inclusion and exclusion criteria. The protocol was accepted by the Regional Ethics Committee of the Community of Madrid. Digitisation of the dental arches was recorded at 3 types of evaluation: 0, 6 months and 12 months. The recording of possible etiologic factors was carried out at the three established evaluation times. The evaluation of satisfaction was recorded at the third evaluation time.

Interventions

OTHERMonitoring (observational study)

The relationship between dental wear and the behaviour of the participants will be analysed.

Sponsors

Universidad Europea de Madrid
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years

Inclusion criteria

* patients over 18 years of age * patients who were to stay at the university for more than one and a half years * patients who agreed to sign the informed consent form.

Exclusion criteria

* pregnant women * patients who planned to modify the oral situation with orthodontic, surgical and/or rehabilitative treatments * patients who had some kind of personal or academic relationship with the investigators of this study.

Design outcomes

Primary

MeasureTime frameDescription
Tooth wear monitoring1 yearQuantification of tissue loss (more than 100 microns) using intraoral scanner related with possible etiological factors

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026