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OpenTrials
Completed

NCT Number: NCT02660216

A Modified Minimally Invasive Approach Towards Le Fort I Osteotomy: a Prospective Study

Nowadays, maxillary Le Fort I osteotomy is a safe and routinely performed procedure. The conventional approach is characterized by a vestibular incision extending from molar-to-molar, associated with a pterygomaxillary disjunction performed with a curved chisel. Adequate mobilization of the maxilla during Le Fort I osteotomy requires an effective separation of the maxillary tuberosity from the pterygoid plates of the sphenoid bone. However, as initially described by Precious (1991) and later by Hernandez-Alfaro (2013), a true pterygomaxillary osteotomy is not necessary to achieve successful disjunction. Furthermore, Hernandez-Alfaro combined his technique of pterygomaxillary disjunction, the so-called "Twist technique", to a minimally invasive protocol, performing the complete Le Fort I osteotomy through a 20 to 30 mm long horizontal vestibular incision. Although promising, the technique remains highly sensitive from a technical standpoint, and its true accuracy has not been comprehensively evaluated.

The purpose of this study is to present and validate a minimally invasive approach towards Le Fort I osteotomy, using a modified pterygomaxillary (PTM) disjunction technique. The primary outcome is to evaluate the accuracy of the technique using rigid voxel-based registration of the 3D virtual treatment planning and the 4 weeks postoperative CBCT images. Secondary outcomes include the surgical time necessary to complete the procedure and the presence of intraoperative and early postoperative complications.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients of all ages
  • Patients of all genders
  • A Le Fort I osteotomy is planned, as part of a bimaxillary orthognathic procedure
  • The surgery is planned with 3D Virtual Treatment Planning (Maxilim v. 2.3.0.3.0.)
  • The planning is transferred with 3D CAD/CAM tooth-borne splint and vertical internal bony reference landmarks
  • The maxilla is repositioned first during the surgery (maxilla first sequence)

Exclusion criteria

  • Patients not eligible according to abovementioned criteria
  • Simultaneous extraction of impacted teeth 18 and/or 28
  • Previous maxillary orthognathic surgery
  • Previous Surgical Assisted Rapid Palatal Expansion (SARPE)
  • Syndromic condition, including cleft lip and palate
  • Segmental Le Fort I osteotomy
  • Adjuvant Zygomatic osteotomy
  • Maxillary impaction higher than 3 mm
  • Maxillary advancement greater than 5 mm

Treatment and study plan

Primary outcomes

  1. accuracy of the minimally invasive approach in comparison to conventional approaches, based on 3D virtual CBCT superimposition of planning CBCT and postoperative CBCT

    Time frame: at 4 weeks postoperative

Secondary outcomes

  1. Surgical time necessary to complete the procedure

    Time frame: perioperative

  2. Intraoperative and early postoperative complications

    Time frame: within 4 weeks postoperative

Sponsors and collaborators

Lead sponsor

AZ Sint-Jan AV

Other

Registry information

Acronym: MILF-I

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Jan 21, 2016
Registry last updated
Jan 19, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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