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.
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.
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.
.
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.
- Conditions
- Orthodontic Patients
- 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 group | Role | What they receive |
|---|---|---|
| skeletally anchored Modified Leaf Expander | Active comparator | 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. Receives: Device: skeletally anchored Modified Leaf Expander |
| Skeletally anchored inverted hyrax | Experimental | 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. Receives: Device: skeletally anchored Modified Leaf Expander |
What is being measured
The primary outcome is the main question the study is designed to answer.
Arch length
Arch length in millimetres
Measured: six months
Inter-canine width
Inter-canine width in millimetres
Measured: six months
Inter-first premolar width
Inter-first premolar width in millimetres
Measured: six months
Inter-second premolar width
Inter-second premolar width in millimetres
Measured: six months
Inter-first molar width
Inter-first molar width in millimetres.
Measured: six months
Secondary outcomes (8)
SNA angle
SNA in degree
Measured: six months
SNB angle
SNB angle in degree
Measured: six months
ANB angle
ANB angle in degree
Measured: six months
FH-MP angle
FH-MP angle in degree
Measured: six months
overjet
overjet in millimetres
Measured: six months
U1/PP
U1/PP (upper incisor to palatal plane) in degree
Measured: six months
L1/MP
L1/MP (lower incisor to mandibular plane) in degree
Measured: six months
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.
- First posted16 Apr 2026
- Study start15 Jan 2024
- Primary completion14 Jul 2025
- Study completion12 Aug 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Orthodontic PatientsStudies of the same condition, open and under way.
- More trials run by Al-Azhar UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Al-Azhar University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mahmoud M. Fathy Aboelmahasen, Al-Azhar University
- Investigators
- Nouran Eissa, Ass. lect, Study chair, Tanta UniversityMohamed Elbialy, Lecturer, Study chair, El mansoura University
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
Study at a glance
From the registry record, last updated by the sponsor on 16 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy of Skeletally Anchored Modified Leaf Expander Versus Modified Conventional Hyrax in Maxillary Molar Distalization: A Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT07534072
- Acronym / sponsor ID
- #R-ORTH-08-25-3220
- Conditions
- Orthodontic Patients
- Keywords
- Maxillary molar, Distalization
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Al-Azhar UniversityUniversity, hospital or other
- Study start
- 15 Jan 2024 (actual)
- Primary completion
- 14 Jul 2025 (actual)
- Study completion
- 12 Aug 2025 (actual)
- First posted
- 16 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
.
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 design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| skeletally anchored Modified Leaf Expander | Active comparator | Device: skeletally anchored Modified Leaf ExpanderThe 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. |
| Skeletally anchored inverted hyrax | Experimental | Device: skeletally anchored Modified Leaf ExpanderFabrication 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. |
Who may qualify
- Ages
- 15 to 18 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (7 listed)
- • Class II molar relation.
Key exclusion criteria (4 listed)
- Congenitally missing teeth
- Congenital anomalies
- Systemic diseases
- Previous orthodontic treatment
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| skeletally anchored Modified Leaf ExpanderAlso: Modified Conventional HyraxIntervention 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 | Device | Skeletally anchored inverted hyrax, skeletally anchored Modified Leaf Expander |
Primary outcome
Arch length
Time frame: six months
Arch length in millimetres
Inter-canine width
Time frame: six months
Inter-canine width in millimetres
Inter-first premolar width
Time frame: six months
Inter-first premolar width in millimetres
Inter-second premolar width
Time frame: six months
Inter-second premolar width in millimetres
Inter-first molar width
Time frame: six months
Inter-first molar width in millimetres.
8 secondary outcomes
SNA angle
Time frame: six months
SNB angle
Time frame: six months
ANB angle
Time frame: six months
FH-MP angle
Time frame: six months
overjet
Time frame: six months
U1/PP
Time frame: six months
L1/MP
Time frame: six months
interincisal angle
Time frame: six months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Apr 2026.
- Individual participant dataSharing planned: No
Related trials for Orthodontic Patients
RecruitingObservational study
Microplastic Exposure From Clear Aligner Wear (MPE)
Microplastic Exposure
Not yet recruiting
Manus AI-Assisted Orthodontic Education and Oral Health-Related Quality of Life
Oral Health-Related Quality of Life
Not yet recruiting
Effectiveness of Personalized Digital Oral Health Intervention in Patients With Fixed Orthodontic Appliances.
Oral Hygiene in Patients With Fixed Orthodontic Appliances, Dental Plaque
Not yet recruiting
Comparison of Orthodontic Molar Protraction With and Without Adjunctive Surgery
Malocclusion
Active, not recruiting
Teleorthodontics Versus Conventional Follow-up During Early Interceptive Orthodontic Treatment in Children
Teledentistry, Orthodontics, Interceptive
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Nouran Eissa, Ass. lect study chair
Tanta University
Mohamed Elbialy, Lecturer study chair
El mansoura University
1 site in 1 country: see every site and its status.
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.