Tooth Wear Monitoring Using Intraoral Scanner

Dental Wear Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05843513
• Other study ID #: Desgaste-UE
• Status: Completed
• Start date: January 18, 2019
• Est. completion date: August 30, 2021

Study information

• Verified date: May 2023
• Source: Universidad Europea de Madrid
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 46
• Est. completion date: August 30, 2021
• Est. primary completion date: January 1, 2021
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

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.

Related Conditions & MeSH terms

• Dental Wear
• Tooth Wear

Intervention

Other:
• Monitoring (observational study)
The relationship between dental wear and the behaviour of the participants will be analysed.

Locations

Country	Name	City	State
Spain	Universidad Europea de Madrid	Villaviciosa De Odón	Madrid

Sponsors (1)

Lead Sponsor	Collaborator
Universidad Europea de Madrid

Country where clinical trial is conducted

Spain, 

References & Publications (2)

Garcia VD, Freire Y, Fernandez SD, Murillo BT, Sanchez MG. Application of the Intraoral Scanner in the Diagnosis of Dental Wear: An In Vivo Study of Tooth Wear Analysis. Int J Environ Res Public Health. 2022 Apr 8;19(8):4481. doi: 10.3390/ijerph19084481. — View Citation

Travassos da Rosa Moreira Bastos R, Teixeira da Silva P, Normando D. Reliability of qualitative occlusal tooth wear evaluation using an intraoral scanner: A pilot study. PLoS One. 2021 Mar 25;16(3):e0249119. doi: 10.1371/journal.pone.0249119. eCollection — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tooth wear monitoring	Quantification of tissue loss (more than 100 microns) using intraoral scanner related with possible etiological factors	1 year