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OpenTrials
Completed

NCT Number: NCT05843513

Tooth Wear Monitoring Using Intraoral Scanner

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.

Completed

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Universidad Europea de Madrid

Villaviciosa de Odón, Madrid, 28670, Spain

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Monitoring (observational study)

Other

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

Primary outcomes

  1. Tooth wear monitoring

    Time frame: 1 year

    Quantification of tissue loss (more than 100 microns) using intraoral scanner related with possible etiological factors

Sponsors and collaborators

Lead sponsor

Universidad Europea de Madrid

Other

Registry information

Official study title

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

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
May 6, 2023
Registry last updated
May 15, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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