Efficacy of Skeletally Anchored Modified Leaf Expander in Maxillary Molar Distalization

April 14, 2026 updated by: Mahmoud M. Fathy Aboelmahasen, Al-Azhar University

Efficacy of Skeletally Anchored Modified Leaf Expander Versus Modified Conventional Hyrax in Maxillary Molar Distalization: A Randomized Clinical Trial

Background:

Distalization in orthodontics is one of conservative treatment modalities that result in gaining space especially in dental orthodontic cases of class ΙΙ molar relationship.

Aim:

This study aimed to compare the distalization effects of the skeletally anchored modified Leaf Expander versus the skeletally anchored modified conventional Hyrax Expander.

Patients and Methods:

Thirty patients (15-18 years) requiring maxillary molar distalization were randomly allocated into two groups (n = 15 each). Group 1 received the modified skeletally anchored self-activated Leaf Expander, and Group 2 received the modified skeletally anchored conventional Hyrax Expander. Pre- and post-distalization lateral cephalometric radiographs and digital dental models were analyzed for skeletal, dental, and arch dimensional changes. Treatment duration and adverse events were also recorded. Statistical analysis included paired t-tests and independent t-tests, with Bonferroni correction (α = 0.0045) applied for multiple comparisons. Effect sizes (Cohen's d) were calculated to assess clinical relevance.

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Study Overview

Status

Completed

Detailed Description

Study setting and populations:

This prospective study included 30 patients consecutively enrolled and treated at the dental clinics, Orthodontic Department, Faculty of Dentistry, Tanta University, Egypt. Patients were aged between 15 and 18 years. All patients underwent maxillary molar distalization using one of two appliances.

Groups' randomization The patients involved in the study groups were randomly distributed through a simple online-generated randomization plan using online software found at the website http://www.graphpad.com/quickcalcs/index. cfm. The allocation ratio is 1:1.

  • Group 1: Patients treated with the modified skeletally supported self-activated Leaf expander as a distalization appliance (7 males, 8 females).
  • Group 2: Patients treated with the modified skeletally supported conventional HYREX expander as a distalization appliance (6 males, 9 females).

Inclusion Criteria

  • Class II molar relation.
  • Patients aged between 15 and 18 years.
  • Overjet less than 6 mm
  • ANB angle between 5° and 7°.
  • Non-extraction treatment plan with molar distalization.
  • Horizontal or normal growth pattern with symmetrical, balanced facial appearance.
  • Minimal crowding in the mandibular arch. Exclusion Criteria
  • Congenitally missing teeth
  • Congenital anomalies
  • Systemic diseases
  • Previous orthodontic treatment Ethical Considerations All patients were informed about the nature, purpose, risks, and benefits of the study prior to enrollment. Written informed consent was obtained from each participant. Patient confidentiality was maintained, and participants retained the right to withdraw at any time without affecting their treatment. Approval for this research was obtained from the Research Ethics Committee, Faculty of Dentistry, Tanta University, Egypt. Under the No. #R-ORTH-08-25-3220.

The Self-Activated Leaf Expander The Leaf Expander (Leaf Expander®, Leone SpA, Sesto Fiorentino, Florence, Italy) resembles a rapid palatal expander but incorporates Nickel Titanium MEMORIA leaf springs that provide continuous force. It consists of two body parts connected by rods over which the leaf springs slide. The springs are held compressed by staples on each side of the body parts. The superelastic nickel-titanium leaf springs deliver a controlled, continuous force once the staples are removed. Two types of Leaf Expanders are available, delivering either 450 or 900 grams of force; the 450-gram/ 6 mm in length version was used in this study.

Intervention Elastic separators were placed mesial and distal to the maxillary first molars bilaterally for 3 days to create space for band placement (19). Appropriate bands were selected and fitted to the molars. An alginate impression was taken with the bands in place, then the bands were removed and repositioned in the impression. The impression was poured in stone to fabricate the working model.

Fabrication of the Modified Palatally Anchored Expander Appliance

The positions of the screws for skeletal anchorage were determined on the model within a safe square on the anterior palatal area. Four lines were drawn (9):

  • The first line, 8 mm distal to the incisive papilla, marked the anterior boundary.
  • The second line, parallel to the first, passed through the distal surfaces of the second premolars to mark the posterior boundary.
  • Two additional lines, each 8 mm lateral to the median palatal raphe, were drawn perpendicular to the first two lines.

The four-point support expander was modified by rotating the line of action 90° to align anteroposteriorly for distalization (9). The distalizer was centered on the palate. The two anterior legs were bent forward and welded to metal sleeves (3 mm diameter) placed 2 mm from the midpalatal raphe. The posterior legs were bent to be welded to the bands on the upper first molars bilaterally. The distalizer was soldered to the bands, finished, polished, and prepared for intraoral insertion

Study outcomes:

The primary outcomes of the current study were: Arch length in millimetres , Inter-canine width in millimetres, Inter-first premolar width in millimetres , Inter-second premolar width in millimetres and Inter-first molar width in millimetres.

While the secondary outcomes were skeletal and dental cephalometric measurements; SNA in degree , SNB in degree , and ANB angles in degree, FH-MP angle in degree, overjet in millimetres , U1/PP (upper incisor to palatal plane) in degree, L1/MP (lower incisor to mandibular plane) in degree, and interincisal angles in degree.

Statistical Analysis

Data were analyzed using Microsoft Excel 2010 and SPSS version 20 (SPSS Inc., Chicago, IL, USA). Numerical data are presented as means ± standard deviations (SD). The Shapiro-Wilk test confirmed normal data distribution. Parametric tests were used for analysis:

  • Paired sample t-tests compared pre- and post-distalization measurements within each group.
  • Statistical significance was set at ( p < 0.05 ).
  • Intraobserver reliability was assessed using the Intra-Class Correlation Coefficient (ICC).

To account for multiple comparisons, a Bonferroni correction was applied. With 11 primary comparisons, the adjusted significance threshold was α = 0.0045. P-values ≤ 0.0045 were considered statistically significant. Effect sizes (Cohen's d) were reported to indicate clinical relevance, even when p-values exceeded the corrected threshold. Clinical relevance (effect sizes) was emphasized alongside strict statistical significance.

Study Type

Interventional

Enrollment (Actual)

30

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

    • Nasr City
      • Cairo, Nasr City, Egypt, 4450113
        • Al- Azhar 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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • • Class II molar relation.

    • Patients aged between 15 and 18 years.
    • Overjet less than 6 mm
    • ANB angle between 5° and 7°.
    • Non-extraction treatment plan with molar distalization.
    • Horizontal or normal growth pattern with symmetrical, balanced facial appearance.
    • Minimal crowding in the mandibular arch.

Exclusion Criteria:

  • Congenitally missing teeth
  • Congenital anomalies
  • Systemic diseases
  • Previous orthodontic treatment

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: skeletally anchored Modified Leaf Expander
The Leaf Expander (Leaf Expander®, Leone SpA, Sesto Fiorentino, Florence, Italy) resembles a rapid palatal expander but incorporates Nickel Titanium MEMORIA leaf springs that provide continuous force. It consists of two body parts connected by rods over which the leaf springs slide. The springs are held compressed by staples on each side of the body parts. The superelastic nickel-titanium leaf springs deliver a controlled, continuous force once the staples are removed. Two types of Leaf Expanders are available, delivering either 450 or 900 grams of force; the 450-gram/ 6 mm in length version was used in this study.

Intervention Elastic separators were placed mesial and distal to the maxillary first molars bilaterally for 3 days to create space for band placement (19). Appropriate bands were selected and fitted to the molars. An alginate impression was taken with the bands in place, then the bands were removed and repositioned in the impression. The impression was poured in stone to fabricate the working model.

Fabrication of the Modified Palatally Anchored Expander Appliance

The positions of the screws for skeletal anchorage were determined on the model within a safe square on the anterior palatal area. Four lines were drawn (9):

  • The first line, 8 mm distal to the incisive papilla, marked the anterior boundary.
  • The second line, parallel to the first, passed through the distal surfaces of the second premolars to mark the posterior boundary.
  • Two additional lines, each 8 mm lateral to the median palatal raphe, were drawn perpendicular to the first two lines.

The four-point support expander was

Other Names:
  • Modified Conventional Hyrax
Experimental: Skeletally anchored inverted hyrax

Fabrication of the Modified Palatally Anchored Expander Appliance

The positions of the screws for skeletal anchorage were determined on the model within a safe square on the anterior palatal area. Four lines were drawn (9):

  • The first line, 8 mm distal to the incisive papilla, marked the anterior boundary.
  • The second line, parallel to the first, passed through the distal surfaces of the second premolars to mark the posterior boundary.
  • Two additional lines, each 8 mm lateral to the median palatal raphe, were drawn perpendicular to the first two lines.

Intervention Elastic separators were placed mesial and distal to the maxillary first molars bilaterally for 3 days to create space for band placement (19). Appropriate bands were selected and fitted to the molars. An alginate impression was taken with the bands in place, then the bands were removed and repositioned in the impression. The impression was poured in stone to fabricate the working model.

Fabrication of the Modified Palatally Anchored Expander Appliance

The positions of the screws for skeletal anchorage were determined on the model within a safe square on the anterior palatal area. Four lines were drawn (9):

  • The first line, 8 mm distal to the incisive papilla, marked the anterior boundary.
  • The second line, parallel to the first, passed through the distal surfaces of the second premolars to mark the posterior boundary.
  • Two additional lines, each 8 mm lateral to the median palatal raphe, were drawn perpendicular to the first two lines.

The four-point support expander was

Other Names:
  • Modified Conventional Hyrax

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Arch length
Time Frame: six months
Arch length in millimetres
six months
Inter-canine width
Time Frame: six months
Inter-canine width in millimetres
six months
Inter-first premolar width
Time Frame: six months
Inter-first premolar width in millimetres
six months
Inter-second premolar width
Time Frame: six months
Inter-second premolar width in millimetres
six months
Inter-first molar width
Time Frame: six months
Inter-first molar width in millimetres.
six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
SNA angle
Time Frame: six months
SNA in degree
six months
SNB angle
Time Frame: six months
SNB angle in degree
six months
ANB angle
Time Frame: six months
ANB angle in degree
six months
FH-MP angle
Time Frame: six months
FH-MP angle in degree
six months
overjet
Time Frame: six months
overjet in millimetres
six months
U1/PP
Time Frame: six months
U1/PP (upper incisor to palatal plane) in degree
six months
L1/MP
Time Frame: six months
L1/MP (lower incisor to mandibular plane) in degree
six months
interincisal angle
Time Frame: six months
interincisal angle in degree.
six months

Collaborators and Investigators

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

Investigators

  • Study Chair: Nouran Eissa, Ass. lect, Tanta University
  • Study Chair: Mohamed Elbialy, Lecturer, El mansoura University

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, 2024

Primary Completion (Actual)

July 14, 2025

Study Completion (Actual)

August 12, 2025

Study Registration Dates

First Submitted

April 2, 2026

First Submitted That Met QC Criteria

April 14, 2026

First Posted (Actual)

April 16, 2026

Study Record Updates

Last Update Posted (Actual)

April 16, 2026

Last Update Submitted That Met QC Criteria

April 14, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • #R-ORTH-08-25-3220

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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