a Comparative Analysis of Subspinal and Conventional Le Fort I Osteotomy on Nasolabial Soft Tissues

April 17, 2026 updated by: Selin Celebi, TC Erciyes University

Evaluation of the Effects of Subspinal Le Fort and Conventional Le Fort I Osteotomy on Nasolabial Soft Tissues

Following surgical operations, patients have aesthetic expectations as well as functional ones. To minimize undesirable aesthetic results after surgery and to increase the effectiveness of the surgery, the surgical method used for maximum aesthetic results is important, both in pre-operative planning and during surgery. In addition, effective control of bleeding and subsequent edema during surgical operations is a high priority for clinical research in surgical applications. Controlling edema and soft tissue damage improves the quality of life of patients after surgery, reduces morbidity and provides greater comfort, and also allows patients to recover quickly and return to their daily activities sooner. Although the developing edema is temporary, it is known to cause serious depressive disorders in some patients. Minimally invasive approach and maximum aesthetic results during surgery are affected by the surgical technique. This study will contribute to the literature by comparing subspinal Le Fort osteotomy with conventional osteotomy.

Study Overview

Detailed Description

In this study, the effect of the type of osteotomy used in the osteotomy phase of orthognathic surgery on the changing parameters (bleeding, edema, soft tissue changes, etc.) during and after surgery will be investigated. While comparing conventional Le Fort I osteotomy with subspinal Le Fort I osteotomy, the advantages and disadvantages of the surgical techniques in the intraoperative and postoperative periods will be determined. This will be the first study to evaluate nasolabial soft tissue changes after subspinal Le Fort osteotomy and to subjectively and objectively compare it with conventional osteotomy performed without v-y closure and cinch sutures, and to evaluate the effect of both methods on postoperative edema. Subspinal Le Fort osteotomy is thought to minimize the widening of the nasal floor. This study has a unique value because it not only evaluates the soft tissue effectiveness of Le Fort osteotomy methods but also provides a three-dimensional comparison of these variables and a subjective explanation. Simultaneously comparing many parameters during and after surgery, and thanks to the results obtained from this study, it will contribute to increasing both the in-operative comfort of oral surgeons and the post-operative comfort of patients. the result of this study, subspinal Le Fort osteotomy will reduce bleeding by reducing dissection during surgery, minimize damage to soft tissues, and prevent unwanted soft tissue changes after surgery.

Study Type

Interventional

Enrollment (Actual)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Talas
      • Kayseri, Talas, Turkey (Türkiye), 38280
        • Erciyes University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • ASA I,
  • without systemic disease,
  • without any drug allergy,
  • and without a history of NSAID use in the week before the operation,
  • patients in both groups did not apply alar cinch suture, V-Y closure, or ANS reduction

Exclusion Criteria:

  • history of cleft lip palate and rhinoplasty

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: CLFI (conventional Le fort I osteotomy )
CLFI was performed as usual Bell WH methods . The maxillary osteotomy was performed from nasal buttress to pterygomaxiller junction by piezosurgery in both groups. Bilateral pterygoid splits were performed with a chisel. After down fracture, bony interferences were removed and maxilla was fixed with miniplates and screws in its new position. ANS repositioning or recounturing, alar cinch suture and V-Y closure were not applied at all.
that performed with conventional Le Fort I
Experimental: SLFI (Subspinal Le Fort I Osteotomy )
SLFI was performed, preventing the pre-existing nasal muscle origins. V-shaped osteotomy at the base of the ANS through a vestibular incision was existed in SLFI. ANS was never exposed to preserve the attachments and periost. Then, the nasal septum and lateral nasal walls were separated by appropriate osteotomes. After this osteotomy, the ANS was separated from the maxilla so that the ANS remains in its former position, hence it is not affected by maxillary movements. To be perpetuated the effectiveness of myrtiformis muscle, that muscle was remained in its former position
Osteotomy was performed in the subspinal Le Fort I group that is described by Mommaerts

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
nasal base width
Time Frame: up to six months

Nasal base width refers to the transverse distance between the most lateral points of the alar bases, reflecting the overall width of the nasal foundation at the level of the nostrils.

Measurement:

It is measured as the linear distance between the right and left alare (al-al) points on frontal view photographs or 3D images, typically using digital calipers or imaging software.

up to six months
alar base width
Time Frame: up to six months

Alar base width is defined as the horizontal distance between the most lateral insertion points of the alar bases where the nostrils meet the cheek.

Measurement:

It is measured as the linear distance between the right and left alare (al-al) landmarks on frontal photographs or 3D stereophotogrammetric images, using calibrated digital software or calipers.

up to six months
upper lip length
Time Frame: up to six months

Upper lip length is defined as the vertical distance between the subnasale and the labiale superius, representing the height of the upper lip in the midline.

Measurement:

It is measured as the linear distance from subnasale (Sn) to labiale superius (Ls) on profile or frontal images using digital measurement software or calipers.

up to six months
nasolabial angle
Time Frame: up to six monts

Nasolabial angle is the angle formed between the columella and the upper lip, reflecting the anteroposterior position and rotation of the nasal tip relative to the upper lip.

Measurement:

It is measured as the angle between a line drawn from subnasale to columella (columellar tangent) and a line from subnasale to labiale superius on lateral profile images or cephalometric analysis.

up to six monts
columellalobular angle
Time Frame: up to six months

Columellalobular angle is the angle formed between the columella and the infratip lobule, reflecting the contour and transition between the nasal tip and columella.

Measurement:

It is measured as the angle between the columellar line and the infratip lobular line on lateral profile photographs or 3D images using digital analysis software.

up to six months
nasal tip angle
Time Frame: up to six months

Nasal tip angle is defined as the angle formed at the pronasale by the intersection of lines extending from the nasion to the pronasale and from the pronasale to the columella, reflecting nasal tip projection and rotation.

Measurement:

It is measured on lateral profile images as the angle between the nasion-pronasale line and the pronasale-columella line using digital software or cephalometric analysis tools.

up to six months
nostril width
Time Frame: up to six months

Nostril width is defined as the maximum horizontal distance across an individual nostril, reflecting the transverse dimension of the nostril aperture.

Measurement:

It is measured as the widest distance between the medial and lateral borders of the nostril on basal view photographs or 3D images using calibrated digital software or calipers.

up to six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
edema
Time Frame: up to six months
Also, the images were used to compare postoperative edema between the groups. To determine even the minutest difference between the two groups, three-dimensional (3D) images were taken at preoperatively and postoperatively on 1, 3, 7, 14, 21, 30 day, 3 month and 6 month after surgery at maximum intercuspidation when the lips were free and the eyes were open
up to six months
rhinoplasty outcome evaluation (roe scale)
Time Frame: up to six months

The Rhinoplasty Outcome Evaluation is a patient-reported outcome measure designed to assess satisfaction with nasal appearance and function following rhinoplasty.

Measurement:

It consists of 6 questions, each scored from 0 (most negative) to 4 (most positive); the total score is summed, divided by the maximum possible score (24), and multiplied by 100 to yield a percentage score ranging from 0 to 100, where higher scores indicate greater patient satisfaction.

up to six months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Mommaerts MY, Abeloos JVS, De Clercq CAS. Comparison of two different techniques to control nasal base width and tip projection in Le Fort I-type osteotomies. J Craniomaxillofac Surg 1994;22:41.
  • Mansour S, Burstone C, Legan H. An evaluation of soft-tissue changes resulting from Le Fort I maxillary surgery. Am J Orthod 1983;84:37-47.
  • Yamashsita Y, Iwai T, Honda K, Fujita K, Imai H, Takasu H, Omura S, Hirota M, Mitsudo K. Effectiveness of subspinal Le Fort I osteotomy in preventing postoperative nasal deformation. Journal of Plastic, Reconstructive & Aesthetic Surgery 2020;73:1326-30.
  • Davidson E, Kumar AR. A preliminary three-dimensional analysis of nasal aesthetics following Le Fort I advancement in patients with cleft lip and palate. Journal of Craniofacial Surgery 2015;26:e629-33.
  • Moragas JSM, Van Cauteren W, Mommaerts MY. A systematic review on soft-to-hard tissue ratios in orthognathic surgery part I: maxillary repositioning osteotomy. Journal of Cranio-Maxillofacial Surgery 2014;42:1341-51.
  • Miloro M, Ghali GE, Larsen PE, Waite PD. Peterson's principles of oral and maxillofacial surgery. vol. 1. Springer; 2004.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2021

Primary Completion (Actual)

December 25, 2021

Study Completion (Actual)

June 15, 2024

Study Registration Dates

First Submitted

April 6, 2026

First Submitted That Met QC Criteria

April 17, 2026

First Posted (Actual)

April 24, 2026

Study Record Updates

Last Update Posted (Actual)

April 24, 2026

Last Update Submitted That Met QC Criteria

April 17, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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