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Clinical Trials/NCT03712007
NCT03712007
Completed
Not Applicable

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

University of Sao Paulo1 site in 1 country35 target enrollmentJune 9, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malocclusion, Angle Class III
Sponsor
University of Sao Paulo
Enrollment
35
Locations
1
Primary Endpoint
Vertical skeletal discrepancy
Status
Completed
Last Updated
4 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
June 9, 2017
End Date
August 10, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Felicia Miranda

DDS, MSc. and PhD Student

University of Sao Paulo

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Vertical skeletal discrepancy

Time Frame: 12 months

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.

Teeth discrepancy

Time Frame: 12 months

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.

Maxillary sagittal skeletal discrepancy

Time Frame: 12 months

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.

Mandibular sagittal skeletal discrepancy

Time Frame: 12 months

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.

Soft tissue discrepancy

Time Frame: 12 months

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.

Secondary Outcomes

  • Maxillary and mandibular inter-first permanent molar distances(12 months)
  • Three-dimensional changes(12 months)
  • Maxillary and mandibular dental arches lengths(12 months)
  • Inclination of maxillary and mandibular first permanent molars(12 months)
  • Discomfort and pain(1 month)
  • Maxillary and mandibular intercanine distances(12 months)
  • Amount of interincisor diastema(7 days)
  • Parents perception of pain(1 month)
  • Maxillary and mandibular dental arches perimeters(12 months)
  • Quality of life evaluation(12 months)

Study Sites (1)

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