Comparison of Two Miniscrew Anchored Maxillary Protraction Protocols

Malocclusion, Angle Class III Clinical Trial

Official title:

Comparison of Two Miniscrew Anchored Maxillary Protraction Protocols: a Randomized Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03712007
• Other study ID #: 67610717.7.0000.5417
• Status: Completed
• Phase: N/A
• Start date: June 9, 2017
• Est. completion date: August 10, 2019

Study information

• Verified date: May 2021
• Source: University of Sao Paulo
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study evaluates the dentoskeletal effects produced by two maxillary protraction protocols in adolescent patients. Half of participants will be treated with a tooth-borne and tooth-bone-borne expanders as anchorage in the maxillary arch. Miniscrews will be used as anchorage in the mandibular arch for both groups.

Description:

Class III malocclusion treatment in growing patients is challenging. A new treatment for maxillary protraction using skeletal anchorage reported an efficient maxillary protraction in the late mixed dentition an early permanent dentition. Therefore, the aim of this study is to compare the dentoskeletal effects produced by two maxillary protraction protocols anchored on miniscrews. The sample will be recruited at the Orthodontic Clinic of Bauru Dental School, University of São Paulo, Brazil. A sample of thirty-five patients, between 9 and 13 years old will be selected. The inclusion criteria are: Class III malocclusion associated with anterior crossbite. The participants will be allocated into 2 groups. Group 1 will comprise 20 individuals treated with a tooth-bone-borne expander and 2 miniscrews in the mandible Group 2 will comprise 15 individuals treated with a tooth-borne expander and 2 miniscrews in the mandible. Digital models and cone-beam computed tomography (CBCT) will be obtained before (T1) and 12 months after treatment (T2). Occlusal radiographs and partial (canine to canine) models will be obtained before and immediately after expansion. Two-dimensional cephalometric evaluations will be performed in the Dolphin® software. The arch width, arch perimeter and arch length will be analyzed with the Orthoanalyzer® software. Three-dimensional superimposition at the cranial base of T1 and T2 CBCT images will be performed. The inter incisor diastema will be evaluated by occlusal radiographs and dental models. Discomfort, pain and quality of life will evaluated by questionnaires. After verifying the normal distribution, the intragroup comparison will be performed with paired t test and intergroup comparison will be performed with t test. In the case of lost to follow-up patients, intention to treat analysis will be used. A significance level of 5% will be regarded for all tests. Temporary pain and discomfort are possible after the installation of the miniscrews. Patients and legal guardians will be informed. After the consent, the treatment can be stoped at any time.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. completion date: August 10, 2019
• Est. primary completion date: August 10, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 9 Years to 13 Years

Eligibility

Inclusion Criteria:

• Both sexes;
• Ages ranging from 9 to 13 years old;
• Class III malocclusion;
• Mandibular canines erupted.

Exclusion Criteria:

• Previous orthodontic treatment;
• Cleft lip and palate;
• Craniofacial syndromes;
• Systemic and/or neurological diseases.

Related Conditions & MeSH terms

• Crossbite (Anterior) (Posterior)
• Malocclusion
• Malocclusion, Angle Class III
• Prognathism

Intervention

Device:
• MAMP therapy with MARPE expander
Twenty patients will be submitted to MAMP therapy with MARPE expander as anchorage in the maxillary arch. The appliance anchorage will be provided by bands adapted on the maxillary first permanent molars and circumferential clamps in the maxillary canines or premolars. The maxillary and mandibular miniscrews will be placed in the same section. After a 24-hour period, parents will be oriented to activate the expander screw. Patients will be instructed to wear intermaxillary elastics connecting the maxillary first molar hooks to the mandibular mini-implants.
• MAMP therapy with Hyrax expander
Fifteen patients will be submitted to MAMP therapy with Hyrax expander as anchorage in the maxillary arch. The appliance anchorage will be provided by bands adapted on the maxillary first permanent molars and circumferential clamps in the maxillary canines or premolars. The mandibular miniscrews will be placed and after a 24-hour period, parents will be oriented to activate the expander screw. Patients will be instructed to wear intermaxillary elastics connecting the maxillary first molar hooks and the mandibular mini-implants.

Locations

Country	Name	City	State
Brazil	University of São Paulo	Bauru	São Paulo

Sponsors (3)

Lead Sponsor	Collaborator
University of Sao Paulo	Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Fundação de Amparo à Pesquisa do Estado de São Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maxillary sagittal skeletal discrepancy	CBCT exams will be obtained before (T1) and after treatment (T2). Reformatted lateral cephalometric images will be obtained using Dolphin software for comparisons with conventional cephalograms. The maxillary sagittal skeletal discrepancy will be observed using the variables: SNA, Co-A, Condylion to ANS and others.	12 months
Primary	Mandibular sagittal skeletal discrepancy	CBCT exams will be obtained before (T1) and after treatment (T2). Reformatted lateral cephalometric images will be obtained using Dolphin software for comparisons with conventional cephalograms. Mandibular sagittal skeletal discrepancy will be observed using the variables: Co-Gn, SNB, Gonial/Jaw Angle and others.	12 months
Primary	Vertical skeletal discrepancy	CBCT exams will be obtained before (T1) and after treatment (T2). Reformatted lateral cephalometric images will be obtained using Dolphin software for comparisons with conventional cephalograms. Vertical skeletal discrepancy will be observed using the variables: Occ Plane to SN, NF - FH (PP-FH), SN - GoGn, SN- Palatal Plane and others.	12 months
Primary	Teeth discrepancy	CBCT exams will be obtained before (T1) and after treatment (T2). Reformatted lateral cephalometric images will be obtained using Dolphin software for comparisons with conventional cephalograms. Teeth discrepancy will be observed using the variables: Overjet, Overbite, Interincisal Angle (U1-L1), Molar Relation, Mesial Molar Relationship, U1 - Palatal Plane, IMPA and others.	12 months
Primary	Soft tissue discrepancy	CBCT exams will be obtained before (T1) and after treatment (T2). Reformatted lateral cephalometric images will be obtained using Dolphin software for comparisons with conventional cephalograms. Soft tissue discrepancy will be observed using the variables: Nasolabial Angle (Col-Sn-UL), Upper Lip to E-Plane, Lower Lip to E-Plane, Upper Lip - S line, Lower Lip - S line and others.	12 months
Secondary	Maxillary and mandibular inter-first permanent molar distances	Arch dimensions will be measured in digital dental models obtained before (T1) and after treatment (T2).	12 months
Secondary	Maxillary and mandibular intercanine distances	The intercanine distance will be measured in digital dental models obtained before (T1) and after treatment (T2).	12 months
Secondary	Maxillary and mandibular dental arches perimeters	Arch perimeter will be measured in digital dental models obtained before (T1) and after treatment (T2).	12 months
Secondary	Maxillary and mandibular dental arches lengths	Arch lenght will be measured in digital dental models obtained before (T1) and after treatment (T2).	12 months
Secondary	Inclination of maxillary and mandibular first permanent molars	Teeth inclination will be measured in digital dental models obtained before (T1) and after treatment (T2).	12 months
Secondary	Amount of interincisor diastema	The interincisor diastema will be measured in the occlusal radiograph and partial model obtained immediately after expansion.	7 days
Secondary	Three-dimensional changes	Three-dimensional changes will be observed by the cranial base superimposition of the CBCT exams obtained before (T1) and after treatment (T2).	12 months
Secondary	Discomfort and pain	Discomfort and pain will be evaluated using a visual analog scale of 10-cm, where 0-cm is no discomfort/pain and 10-cm is the greatest discomfort/pain.	1 month
Secondary	Parents perception of pain	Parents perception of pain will be evaluated using a visual analog scale of 10-cm, where 0-cm is no discomfort/pain and 10-cm is the greatest discomfort/pain.	1 month
Secondary	Quality of life evaluation	CPQ (Child Perceptions Questionnaires) will be used to evaluated quality of life. The CPQ8-10 and CPQ11-14 will be applied before (T1), during and after (T2) treatment for patients of both groups.	12 months