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Orthodontic Extrusion of High Risk Impacted Mandibular Third Molar

Not Applicable
Completed
Conditions
Inferior Alveolar Nerve Injuries
Interventions
Procedure: Orthodontic extrusion of the impacted mandibular third molar by using the maxillary miniscrew and cross arch elastic power chain as a temporary anchorage device before extraction
Registration Number
NCT06538688
Lead Sponsor
Alexandria University
Brief Summary

The goal of this clinical trial is to investigate the usage of maxillary miniscrew and cross-arch elastics for the orthodontic traction of the impacted mandibular third molar in close proximity to the inferior alveolar nerve to decrease the chance of nerve injury

Detailed Description

To investigate the traction of the impacted mandibular third molar away from the inferior alveolar nerve by using the orthodontic miniscrew in the maxillary bone and cross-arch elastic power chain as a temporary anchorage device before extraction to avoid injury of the nerve and neurosensory complications.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
9
Inclusion Criteria
  • patients with impacted mandibular third molar in close proximity to the inferior alveolar nerve.
  • Cooperative patients free of chronic diseases which interfere with needed results (e.g.diseases affect the bone regeneration ).
  • Patients with good oral hygiene.
Exclusion Criteria
  • patients with limitation in mouth opening.
  • patients with mental or physical disabilities.
  • Allergy to anaesthetic components or antibiotics.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
ParticipantsOrthodontic extrusion of the impacted mandibular third molar by using the maxillary miniscrew and cross arch elastic power chain as a temporary anchorage device before extractionPatients with impacted mandibular third molar in close proximity to the inferior alveolar nerve
Primary Outcome Measures
NameTimeMethod
Radiographically6months

By measuring the amount of extrusion of the impacted tooth gained in millimetres Using CBCT

Secondary Outcome Measures
NameTimeMethod
clinical brush stroke directional test6months

using a micro brush tip which was moved in horizontal and/or vertical directions on the chin area ten times and asked the patient to reproduce the movements the scale ranged from 0-2, where 0= no sensation, 1= decreased sensation and 2= normal sensation.

Clinical neurosensory assessment6months

By using pinprick test in which ;A sharp dental probe was applied to the skin over chin region, lip and mucosa in a quick pricking movement and pain perception of the patient was assessed. Each area was tested three times bilaterally.the scale ranged from 0-2, where 0= no sensation, 1= decreased sensation and 2= normal sensation.

Clinical Two-point discrimination test6months

By using probes of caliper device which were drawn across the skin at constant pressure and patient was asked whether one or two points were felt, the minimum separation distance was felt by the patient was termed two point discrimination threshold.scoring from 0-2 in which; 0=\>15mm, 1=8-15, 2= \<8 .

Trial Locations

Locations (3)

Alexandria university

🇪🇬

Alexandria, Egypt

Faculty of Dentistry, Alexandria University

🇪🇬

Alexandria, Egypt

Faculty of Dentistry

🇪🇬

Alexandria, Egypt

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