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Assessment of Vertical Pattern in Correlation With Third Molar Inclusion : A 3D CBCT Analysis

C

Central Hospital, Nancy, France

Status

Enrolling

Conditions

Impacted Third Molar Tooth

Treatments

Other: Radiographic measurement

Study type

Observational

Funder types

Other

Identifiers

NCT06320665
2024PI003

Details and patient eligibility

About

The objective is to compare the sagittal and vertical skeletal parameters of patients with an impacted third molar.

Patients will be analyzed according to their skeletal characteristics: skeletal class (sagittal direction) and facial skeletal typology (vertical direction).

The inclusion characteristics of third molars will also be analyzed, to see the links between typology and inclusion. The principal hypothesis is no significant difference in third molar inclusion patterns in relation to skeletal divergence.

Full description

The study is a non-interventional (observational) research involving the human person, research on existing data (retrospective study) and samples dealing with dentofacial orthopedics.

This study analyzes third molar inclusion patterns in relation with the skeletal characteristics, sagittal and vertical typology.

This is a comparative retrospective study of radiographs in three dimensions before any orthodontic treatment. The patients studied are at Bacchetti CS stage 5 (adults), and the third molar must be at least at Nolla stage 6 of formation.

There is no control group but there are subgroups depending of the skeletal characterics.

Enrollment

80 estimated patients

Sex

All

Ages

15+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • CMV stage 5 on lateral radiography (end of growth)
  • at least one impacted third molar at minimum Nolla stage 6 development

Exclusion criteria

  • Previous maxillofacial trauma
  • Growing patients
  • Missing permanent tooth or early avulsion
  • Dysplasia
  • Dentofacial deformities
  • Endocrinological pathologies with implications for maxillofacial growth
  • Syndromes
  • History of maxillofacial or orthognathic surgery
  • History of orthodontic treatment
  • Incomplete data

Trial design

80 participants in 3 patient groups

Class I
Description:
Patient with class I occlusion, with at least one impacted third molar
Treatment:
Other: Radiographic measurement
Class II
Description:
Patients with class II malocclusion, with at least one impacted third molar
Treatment:
Other: Radiographic measurement
Class III
Description:
Patients with class III malocclusion, with at least one impacted third molar
Treatment:
Other: Radiographic measurement

Trial contacts and locations

1

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Central trial contact

Mathilde LAE; Bart VANDE VANNET, PhD

Data sourced from clinicaltrials.gov

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