Malocclusion, Angle Class I, Malocclusion; Angle Class II Division 1
Conditions
Keywords
Accelerated orthodontic tooth movement (AOTM), Peizo-corticission
Brief summary
The purpose of this study is to provide evidence on the effectiveness, the efficiency and efficacy of Peizo-Corticission in accelerating orthodontic tooth movement and reducing orthodontic treatment time.
Detailed description
1 Aim of the study- Part I: This prospective controlled clinical trial (CCT), Split Mouth Design is conducted to assess the efficiency of piezo-corticision in accelerating tooth movement and in reducing treatment time during retraction of canine teeth in class II div 1 subjects. Specific aim- Part I: A- To compare rate of tooth retraction between piezo-corticised and the conventionally orthodontically moved canines B- To compare length of treatment of both approaches. 2- Objectives of the Study Part II: This prospective randomized controlled clinical trial (RCT) is designed to assess the efficiency of piezo-corticision in accelerating tooth movement and in reducing treatment time during retraction of anterior teeth in class II div 1 and class 1 bi-maxillary protrusive subjects. Specific aim Part II: 1. To compare rate of tooth retraction between piezo-corticised and the conventionally orthodontically moved incisors 2. To compare length of treatment of both approaches. 3. To evaluate the quality of treatment outcome of both treatment approaches according to American Board of Orthodontics (ABO) standards.
Interventions
PROCEDUREPeizocorticision
Peizocorticision a non invasive procedure used in/ to accelerate orthodontic tooth movement
PROCEDUREConventional Orthodontic Mechanics
Full Fixed Orthodontic Appliance with conventional orthodontic Mechanics
Sponsors
King Abdullah International Medical Research Center
AL Yousef
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
15 Years to 35 Years
Healthy volunteers
Yes
Inclusion criteria
Study Subjects for Part I and Part II: Inclusion: * Voluntary participation of patients only * Able to follow instruction, able to understand the consent form and sign it. * Adult Female and Male Saudi patients 15-35 y.o * Subjects who are none smokers * Subjects with good health according to American Society of Anesthesiology ASA-I with full permanent dentition regardless of the third molars. * Subjects with good periodontal and gingival health: Gingival Index GI≤ 1 * Subjects with a none gummy smile, * Subjects with full complement of permanent caries-free dentition; Restored teeth should be of proper sound intact fillings * Subjects without root anomalies * Subjects with mild-moderate skeletal and dental cephalometric measurements: OB ≤ 40%, OJ ≤ 6, ANB ≤ 5 °, SN-GOGN ≤ 29 °, Subjects' dentition Angle classification class II div 1, 3mm molar and canine occlussal relationship; and subjects with class 1 Bi-maxillary protrusion Exclusion: * Subjects younger than 15 y.o * Subjects who cannot comprehend the surgical procedure and who cannot consent for themselves * Subjects who are medically classified as ASA-II, III * Subjects who are taking any systemic or local medications especially Insulin, non-steroidal anti-inflammatory drugs, bisphosphonate, corticosteroids * Subjects who are pregnant * Subjects who are smokers * Subjects with craniofacial syndromes: cleft lip and palate; or facial trauma * Subjects with unhealthy or compromised periodontium * Subjects with a gummy smile * Subjects with inadequately treated endodontic and dental fillings problems * Subjects with previous root resorption or dental developmental anomalies * Subjects who had previous orthodontic treatment * Subjects with TMJ signs and symptoms; Mandibular functional shift * Subjects with extreme skeletal and dental class II: SN-GOGN ≥ 32°, OJ ≥ 6mm * Subjects will be excluded if broken brackets or lost coils which have not been replaced immediately within few days from breakage or loss. * Subjects will be excluded if any of mini-screws failed during treatment * Subjects who become medically unfit during course of trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of orthodontic canine movement | 4-6 months |
Secondary
| Measure | Time frame |
|---|---|
| Rate of orthodontic Incisor Retraction | 4-6 months |
Countries
Saudi Arabia
Contacts
Primary ContactSally K Al-Yousef, Msc-Ortho
Outcome results
None listed