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Trueness of Digital Occlusal Analysis

A

Alexandria University

Status

Active, not recruiting

Conditions

Occlusal Analysis
Dental Occlusion

Study type

Observational

Funder types

Other

Identifiers

NCT06672627
0974-09

Details and patient eligibility

About

The aims of this observational study are to evaluate the trueness of two different digital occlusal analyzers; handheld occlusal analyzer versus intraoral scanner in comparison to conventional methods in identifying true occlusal contacts and to evaluate inter-examiner reliability of two examiners independently analyzing occlusal contacts.

Full description

Evaluate the trueness of two different digital occlusal analyzers; handheld occlusal analyzer (occlusense) versus intraoral scanner (Medit i700-medit occlusal analyzer) in comparison to conventional methods (8 um articulating paper) in identifying true occlusal contacts and to evaluate inter-examiner reliability of two examiners independently analyzing occlusal contacts.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Normal occlusion (Angle Class 1)
  • No missing teeth
  • No tempromandibular disorders

Exclusion criteria

Patients having:

  • Dental prostheses
  • Extensive restorations
  • Severe malocclusion
  • Periodontal disease
  • Excessive tooth wear
  • Orofacial pain
  • Temporomandibular joint disorders
  • Anterior or posterior open bite
  • Active orthodontic treatment.

Trial design

30 participants in 3 patient groups

Control group
Description:
Every participant will undergo occlusal analysis using conventional methods (8um articulating paper)
Study group I
Description:
Every participant will undergo digital occlusal analysis using hand held device (occlusense)
Study group II
Description:
Every participant will undergo digital occlusal analysis using intraoral scanner (Medit occlusal analyzer)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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