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OpenTrials
Completed

NCT Number: NCT00904930

Evaluation of the Periotest Method in Dental Traumatology

Background/Aims: The Periotest® method represents a technique for objective tooth mobility assessment. The aims of this study were: 1. receiving information about normal Periotest® values in vertical and horizontal dimension on periodontally healthy teeth for individuals aged 20-35, 2. investigating the reliability of the Periotest® method in terms of intra-serial and inter-serial reproducibility before splinting and with an applied dental trauma splint, 3. evaluating the splint effect of two different wire-composite splints in vivo.

Materials and Methods: On periodontally healthy dental students (n=33; mean age 24.7 years) Periotest® values were measured on reproducible measuring points, in vertical and horizontal dimension and before splinting and after splint insertion. Three readings were taken per serial to observe the intra-serial reproducibility, and for testing inter-serial reproducibility three serials were measured (Friedman-test; P ≤ 0.001). Two different wire-composite-splints (1 = Dentaflex 0.45 mm, 2 = Strengtheners 0.8x1.8) were inserted, the Periotest® values were measured and the splint effects were calculated and compared (Whitney-Mann-U-test; P ≤ 0.001).

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Key information

Conditions

Age range

19 year–36 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Friedrich-Alexander-University Erlangen-Nuremberg

Erlangen, Bavaria, 91054, Germany

Who can participate

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

Inclusion criteria

  • age 19-36
  • healthy upper front teeth

Exclusion criteria

  • periodontal disease
  • orthodontic treatment during the investigation period
  • history of dental trauma
  • fillings or restorations on upper front teeth
  • endodontically treated teeth

Treatment and study plan

Wire Composite Splint (Dentaflex 0.45 mm)

Device

Wire-Composite-Splint: Dentaflex 0.45 mm (Dentaurum, Pforzheim, Germany) attached with Tetric flow (IvoclarVivadent, Schaadn, Liechtenstein) to the teeth

Wire Composite Splint (Denture Strengtheners)

Device

Wire-Composite-Splint: Denture Strengtheners 0.8x1.8 mm (Dentaurum, Pforzheim, Germany) attached with Tetric flow to the teeth

Sponsors and collaborators

Lead sponsor

University of Erlangen-Nürnberg Medical School

Other

Registry information

Official study title

Evaluation of the Periotest Method as a Tool for Tooth Mobility Monitoring and Splint Rigidity Assessment in Dental Traumatology

Important dates

First posted
May 20, 2009
Registry last updated
Dec 14, 2020

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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