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Finite Element Modelling of Le Fort I Osteotomy Fixation : PSI vs Miniplates

C

Centre Hospitalier Universitaire de Nice

Status

Not yet enrolling

Conditions

Malocclusion

Treatments

Other: In silico orthognathic surgery with customized implants digital only on 3D scanners

Study type

Observational

Funder types

Other

Identifiers

NCT07365657
26IUFC01

Details and patient eligibility

About

This study aimed to evaluate the biomechanical performance of patient-specific versus conventional fixation for Le Fort I osteotomy using subject-specific finite element models derived from real surgical plans. Two distinct clinical scenarios-a minor advancement without impaction and a moderate advancement with posterior impaction-were analyzed to determine how surgical movements influence implant stress, bone stress, and maxillary micromotion. By combining surgical planning with validated computational modeling, this work provides clinically relevant insight to optimize PSI design and guide fixation strategy selection in orthognathic surgery.

Enrollment

2 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient operated on By Pr SAVOLDELLI.
  • Patient undergoing patient-specific orthognathic surgery.
  • Access to numerical (digital) planning.

Exclusion criteria

  • Previous maxillo-facial trauma.
  • Facial cleft.

Trial design

2 participants in 2 patient groups

Type II maloclusion
Description:
2 patients : one with type II maloclusion, one with type III maloclusion who previously undergone orthognathic surgery
Treatment:
Other: In silico orthognathic surgery with customized implants digital only on 3D scanners
Type III maloclusion
Description:
2 patients : one with type II maloclusion, one with type III maloclusion who previously undergone orthognathic surgery
Treatment:
Other: In silico orthognathic surgery with customized implants digital only on 3D scanners

Trial contacts and locations

1

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Central trial contact

Olina Rios; Charles +33 SAVOLDELL

Data sourced from clinicaltrials.gov

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