Menu
Not yet recruiting NCT06668779

Digital Analysis of Primary Teeth Dimensions in a Group of Egyptian Children (4-6 Years)

Observational Digital Analysis of Tooth Crown Dimensions of Primary Teeth

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Digital Analysis of Tooth Crown Dimensions of Primary Teeth. Basic parameters: 4 years — 6 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Digital Analysis of Tooth Crown Dimensions of Primary Teeth in a Group of Egyptian Children (4-6 Years) : (A Cross Sectional Study)

Overview

Tooth size (Mesiodistal, Buccolingual and Occluso-gingival) has an important role in pediatric dentistry as it helps for fabrication of appropriate sizes of zirconia crowns for primary anterior teeth and Stainless-Steel crowns for primary posterior teeth. Tooth size differs among and within populations.

Primary outcome measures

  • tooth crown dimensions of primary teeth [Time frame: 8 months]

Eligibility criteria

Inclusion criteria

  • Children aged 4-6 years
  • Fully erupted first and second primary molars
  • Sound interproximal \& buccal / lingual walls with or without minimal occlusal pits \& fissure incipient caries.
  • No previous interproximal \& buccal / lingual restorations
  • Intact mesial and distal marginal ridge

Exclusion criteria

  • Children with gross carious lesions.
  • Children with hypo-mineralization, hypoplasia and fracture.
  • Children with mental disability.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06668779 · Digital analysis of dimensions

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗