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Orthodontic PatientsNCT07534072

Efficacy of Skeletally Anchored Modified Leaf Expander in Maxillary Molar Distalization

A study testing skeletally anchored Modified Leaf Expander in people with Orthodontic Patients, run by Al-Azhar University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 15 to 18 yearsHealthy volunteers can take part
Conditions the study is for
Orthodontic Patients
What is being tested?
skeletally anchored Modified Leaf Expander
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteEgypt
Study dates
15 Jan 2024to 12 Aug 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 18 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • • 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.

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Al- Azhar University

    Cairo, Nasr City, 4450113

Other trials in Egypt

About this study

Official title: 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.

Read more

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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Read the 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.

Being tested
skeletally anchored Modified Leaf Expander
Keywords
Maxillary molar, Distalization

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • skeletally anchored Modified Leaf ExpanderDevice

    Also called Modified Conventional Hyrax

    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

Study groups in NCT07534072
Study groupRoleWhat they receive
skeletally anchored Modified Leaf ExpanderActive comparatorThe 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.
Receives: Device: skeletally anchored Modified Leaf Expander
Skeletally anchored inverted hyraxExperimentalFabrication 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.
Receives: Device: skeletally anchored Modified Leaf Expander

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Arch length

    Arch length in millimetres

    Measured: six months

  2. Inter-canine width

    Inter-canine width in millimetres

    Measured: six months

  3. Inter-first premolar width

    Inter-first premolar width in millimetres

    Measured: six months

  4. Inter-second premolar width

    Inter-second premolar width in millimetres

    Measured: six months

  5. Inter-first molar width

    Inter-first molar width in millimetres.

    Measured: six months

Secondary outcomes (8)
  1. SNA angle

    SNA in degree

    Measured: six months

  2. SNB angle

    SNB angle in degree

    Measured: six months

  3. ANB angle

    ANB angle in degree

    Measured: six months

  4. FH-MP angle

    FH-MP angle in degree

    Measured: six months

  5. overjet

    overjet in millimetres

    Measured: six months

  6. U1/PP

    U1/PP (upper incisor to palatal plane) in degree

    Measured: six months

  7. L1/MP

    L1/MP (lower incisor to mandibular plane) in degree

    Measured: six months

  8. interincisal angle

    interincisal angle in degree.

    Measured: six months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Apr 2026
  2. Study start15 Jan 2024
  3. Primary completion14 Jul 2025
  4. Study completion12 Aug 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07534072
Sponsor's protocol ID
#R-ORTH-08-25-3220
Status last verified
Apr 2026
First submitted
2 Apr 2026
Last updated
16 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing skeletally anchored Modified Leaf Expander in people with Orthodontic Patients, run by Al-Azhar University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Arch length (time frame: six months). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Apr 2026.

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