Evaluation of the Periotest Method in Dental Traumatology
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Purpose
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).
| Condition | Intervention |
|---|---|
|
Dental Trauma |
Device: Wire Composite Splint (Dentaflex 0.45 mm) Device: Wire Composite Splint (Denture Strengtheners) |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Cross-Sectional |
| Official Title: | Evaluation of the Periotest Method as a Tool for Tooth Mobility Monitoring and Splint Rigidity Assessment in Dental Traumatology |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
no periodontal disease
33 dental students (13 male, 20 female) with a mean age of 24.7 years (min. 19.8; max. 36.5) with no periodontal disease or dental trauma
|
Device: Wire Composite Splint (Dentaflex 0.45 mm)
Wire-Composite-Splint: Dentaflex 0.45 mm (Dentaurum, Pforzheim, Germany) attached with Tetric flow (IvoclarVivadent, Schaadn, Liechtenstein) to the teeth
Device: Wire Composite Splint (Denture Strengtheners)
Wire-Composite-Splint: Denture Strengtheners 0.8x1.8 mm (Dentaurum, Pforzheim, Germany) attached with Tetric flow to the teeth
|
Eligibility| Ages Eligible for Study: | 19 Years to 36 Years |
| Genders Eligible for Study: | Both |
| Sampling Method: | Non-Probability Sample |
Dental students Dental Clinic 1 and 2
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
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00904930 History of Changes |
| Other Study ID Numbers: | PT-WCS1-WCS2-Hu |
| Study First Received: | May 19, 2009 |
| Last Updated: | May 20, 2009 |
| Health Authority: | Germany: Ethics Commission |
Keywords provided by University of Erlangen-Nürnberg Medical School:
|
Tooth mobility assessment Splinting Splint Rigidity |
Additional relevant MeSH terms:
|
Tooth Mobility Periodontal Diseases Mouth Diseases Stomatognathic Diseases |
ClinicalTrials.gov processed this record on May 21, 2013