- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06486324
Effects of Asymmetric Rapid Maxillary Expansion on Dentoskeletal Structures in Mixed Dentition (ARME)
Investigation of the Effects of Rapid Maxillary Expansion With Locked Modified Acrylic Bonded Appliance on Dentofacial Structures in Mixed Dentition
Study Overview
Status
Intervention / Treatment
Detailed Description
A posterior crossbite (PCB) is defined as an abnormal transverse or inverse relationship between the posterior teeth and dentition of the upper and lower jaws. A full buccal segment PCB involves multiple teeth in the posterior dentition and usually represents a transverse size discrepancy between the maxillary and mandibular relationships. This discrepancy is often caused by narrow or underdeveloped transverse dimensions of the maxillary halves. The underlying etiology of PCBs includes congenital, developmental, traumatic, or iatrogenic causes. Since spontaneous correction of this malocclusion is not possible even if the etiological factors are eliminated, it should be treated with maxillary expansion as early as possible.
The PCBs may be seen a unilateral posterior crossbite (UPCB) or bilateral posterior crossbite during all periods of dentition. A UPCB can be described as a functional UPCB or true UPCB. A functional UPCB is usually associated with a lateral shift of the mandible toward the crossbite side during the transition of the mandible. On the other hand, true UPCB is less common than functional UPCB and is caused by the narrowing of one of the maxillary halves. Increasing the maxillary arch transverse dimension is the main goal in the treatment of PCB. Although bilateral maxillary expansion is usually used to symmetrically widen the maxillary arch and eliminate mandibular shift as a standard treatment model in functional PCB, asymmetrical or unilateral maxillary expansion is recommended to expand narrowed sections of the maxillary halves and prevent overexpansion of the non-crossbite side in the treatment of true UPCB. Therefore, several removable or fixed maxillary expansion appliances that are slowly or rapidly activated were modified to produce differential effects on posterior teeth.
This clinical trial was designed to expand the upper jaw asymmetrically, i.e. to prevent the normal side of the bite from expanding while expanding the narrow part of the upper jaw. For this purpose, a locking mechanism was added to a bonded rapid maxillary expansion (RME) appliance to support the lower posterior teeth on the normal side of the bite.The hypothesis tested in the study was whether the true unilateral posterior cross-bite in the mixed dentition period could be corrected with a locked modified bonded rapid maxillary expansion appliance used for asymmetric expansion.
Children aged between 7 and 10 years old with true unilateral posterior crossbite were enrolled in the study. The efficacy of the appliance was compared between the crossbite and non-crossbite sides in the patients included in the study. The crossbite side of the patients was assigned as the treatment group, while the normal bite or noncrossbite side was assigned as the positive control group. Thus, two groups were formed for the study, and the trial was conducted on these groups.In other words, the study was planned as a self-controlled study. A negative control group could not be formed due to ethical reason. The reason for this is that the transversal problem may negatively affect both the anterioposterior and vertical development of the jaws in patients of this age during the developmental period, and therefore it was deemed necessary to correct the cross-bite problem as soon as possible after it was detected.Therefore, the purpose of this study was to evaluate specific dentoskeletal changes induced by treatment with true UPCB in mixed dentition with asymmetric RME.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- mixed dentition
- true unilateral posterior crossbite
- erupted first permanent molars and incisors
- all deciduous canines and molars or no more than one missing deciduous molar
- no history of orthodontic treatment
- no systemic disease
- no pathological periodontal status
- no excessive gagging reflex.
Exclusion Criteria:
- poor oral hygiene
- caries
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment Group
Crossbite Side
|
asymmetric maxillary expansion
Other Names:
|
|
Experimental: Positive Control Group
Non-cossbite Side
|
asymmetric maxillary expansion
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Widths of skeletal structures
Time Frame: Before expansion (T1),through expansion completion,an average 1 month (T2),and through retention completion, an average 3 months (T3)
|
The widths of the nasal cavity, maxilla and mandible were measured in millimetres on the frontal radiographs and these widths were also determined separately on both the crossbite and non-crossbite sides.This involved marking anatomical points (lateral piriform rim,jugale, gonial notch and Lo points on both sides of the face and crista galli, a single point) and drawing two reference lines.The horizontal reference line was drawn by connecting the Lo points on both sides.The perpendicular line drawn from the crista galli to the horizontal reference line was the midsagittal line, which divided the face into two separate halves.The distances between the inter lateral piriform points, the inter jugular points and the inter gonial points corresponded to the width of the nasal cavity, the maxillary width and the mandibular width, respectively.The distances between the anatomical points on one half of the face to the midsagittal line indicated the skeletal width on that side.
|
Before expansion (T1),through expansion completion,an average 1 month (T2),and through retention completion, an average 3 months (T3)
|
|
Skeletal maxillomandibular width ratios
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
The skeletal maxillomandibular ratio was calculated by dividing the skeletal maxillary width by the skeletal mandibular width and multiplying the result by 100.
This percentage was calculated separately for the crossbite and non-crossbite sides and also for the total maxillary and mandibular width.
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Inclinations of upper and lower first molars
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
The angle formed by the intersection of the horizontal reference line with the line indicating the axis of a molar tooth defines the angular inclination of the molar tooth.
The line indicating the axis of a molar was defined by the line connecting the crest of the buccal tubercle of the tooth and the most external part of the buccal curvature of the crown on the frontal radiograph.
The angular inclinations of the upper and lower first molars were measured in degrees on frontal radiographs.
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Amount of movement of deciduous canines and first molars in the transversal plane on the crossbite and non-crossbite sides.
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
The perpendicular distances of deciduous canines and permanent first molars on the crossbite and non-crossbite sides to the median plane (MP), which was established as the reference plane on the dental cast.
Distance measurements of the teeth were made in millimeter and these measurements represent the amount of movement of the canines and molars in the transverse plane.
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Intercanine and intermolar distance on dental cast
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
The distance measurement between the deciduous canines in the transversal plane on the upper and lower dental casts (intercanine distance).
The distance measurement between the permanent first molars in the transversal plane on the upper and lower dental casts (intermolar distance).
Distance measurements of the teeth were made in millimeter.
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Position of the maxilla in the sagittal and vertical plane on lateral cephalometric radiography
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
1) SNA angle:The angle formed between the anterior cranial base (SN plane) passing through the Sella (S) and Nasion (N) points and the NA plane passing through the N and A points.It shows the sagittal position of the maxilla in degrees.2)SV⊥A
(mm): The perpendicular distance of point A to the Sella Vertical (SV) line.
SV was constructed through the Sella, perpendicular to the SN plane.
It gives the position of the maxilla in the sagittal direction in millimetres.3)SN-PP
angle: The angle formed between the SN plane and the palatal plane (PP) passing through the anterior nasal spine (ANS) and posterior nasal spine (PNS).It shows the vertical position of the maxilla and maxillary rotation in degrees.4)SN⊥ANS
(mm): The perpendicular distance of ANS to SN plane.
It gives the position of the ANS in the vertical position in millimetres.5)SN⊥PNS
(mm): The perpendicular distance of PNS to SN plane.
It gives the position of the PNS in the vertical direction in millimetres.
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Position of the mandibula in the sagittal and vertical plane on lateral cephalometric radiograph
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Maxillomandibular relationship in the sagittal plane on lateral cephalometric radiograph
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
ANB angle: The angle formed between the NA and NB planes.
It shows the positions of the maxilla and mandible relative to each other in the sagittal direction in degrees.
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Skeletal midface and lower face heights in vertical plane on lateral cephalometric radiograph
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Angulation and position of the upper central incisor on lateral cephalometric radiograph
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Angulation and position of the lower central incisor on lateral cephalometric radiograph
Time Frame: Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
|
Before expansion(T1),through expansion completion an average 1 month(T2),and through retention completion an average 3 months(T3)
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Celal Irgın, Asst.Prof., Selcuk University
Publications and helpful links
General Publications
- Toroglu MS, Uzel E, Kayalioglu M, Uzel I. Asymmetric maxillary expansion (AMEX) appliance for treatment of true unilateral posterior crossbite. Am J Orthod Dentofacial Orthop. 2002 Aug;122(2):164-73. doi: 10.1067/mod.2002.125563.
- da Silva Filho OG, Boas MC, Capelozza Filho L. Rapid maxillary expansion in the primary and mixed dentitions: a cephalometric evaluation. Am J Orthod Dentofacial Orthop. 1991 Aug;100(2):171-9. doi: 10.1016/s0889-5406(05)81524-0.
- Sari Z, Uysal T, Usumez S, Basciftci FA. Rapid maxillary expansion. Is it better in the mixed or in the permanent dentition? Angle Orthod. 2003 Dec;73(6):654-61. doi: 10.1043/0003-3219(2003)0732.0.CO;2.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 08102026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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