Malocclusion, Angle Class II, Division 1
Conditions
Keywords
Orthodontic Tooth Movement Acceleration
Brief summary
The long time needed for orthodontic treatment is considered one of the biggest obstacles that make patients refuse to undergo orthodontic treatment. It also has many disadvantages including higher caries rates, gingivitis, and root resorption. Therefore, the purpose of this study is to evaluate the efficiency of two new noninvasive methods (Low-Level Laser Therapy and Corticopuncture) in accelerating orthodontic tooth movement for the implant supported En-Masse retraction of the six maxillary anterior teeth.
Detailed description
This study will be a randomized controlled trial with a 1:1:1 allocation ratio. Sample size was calculated using Minitab version 15. 36 Participants recruited from patients attending the Department of Orthodontics and Dentofacial Orthopedics at Damascus University with class II division 1 malocclusion that indicates the extraction of first maxillary premolars will be randomly assigned into one of three groups: Low-Level Laser Therapy (LLLT) group, flapless corticopuncture group, or control group. Titanium mini-implants (1.6 mm diameter and 7 mm length) will be inserted between the maxillary second premolar and first molar at approximately 8-10 mm height above the archwires below the mucogingival junction. After complete leveling and alignment of the maxillary dental arch, which will be defined by passive insertion of 19\*25 inch S.S. archwire, the retraction stage of the six maxillary anterior teeth will begin.
Interventions
RADIATIONLow-Level Laser Therapy (LLLT)
LLLT will be applied in this group
PROCEDUREFlapless Corticopunture
Small holes in the cortical bone will be achieved using 1-mm diameter round surgical Tungsten bur
OTHERControl
Typical orthodontic treatment with no LLLT or flapless corticopuncture
Sponsors
Damascus University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 24 Years
Healthy volunteers
No
Inclusion criteria
1. Patient age between (18 - 24) years. 2. Class II Division 1 malocclusion that indicates extraction of two maxillary first premolars with the following parameters: ANB: 5 to 10 degrees. Overjet: 5 to 10 mm. Growth Pattern: normal or slightly vertical. 3. All upper teeth are existed (Except for third molars). 4. Mild to moderate crowding (3 mm or less). 5. Patient dose not undergo any medical treatment that interfere with orthodontic tooth movement (Cortisone, NSAIDs, …). 6. Good oral hygiene (Plaque index \< 1).
Exclusion criteria
1. Any medical condition affecting orthodontic tooth movement. 2. Poor oral hygiene (Plaque index \> 1). 3. Patient did not undergo previous orthodontic treatment. 4. Patient lack of commitment toward follow-up appointments.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Duration of en-masse retraction of the six maxillary anterior teeth | The months required to complete the retraction procedure will be recorded, which is expected to be occur within four months | Assessment will be performed by calculating the time required from the beginning of the six maxillary anterior teeth retraction till the completion of this procedure |
| Rate of en-masse retraction of the six maxillary anterior teeth | The calculation of the rate of retraction will be done once the retraction procedure has finished which is expected to occur within four months | Assessment will be performed on study models by dividing the distance that the six maxillary anterior teeth moved during retraction to the time required to retract them to their ideal positions. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the gingival indices | This outcome will be measured one day before the six maxillary incisors retraction initiation (T0) and immediately after the completion of retraction (T1) which is expected to occur in 4 months | Assessment will be performed clinically using the WHO probe |
| Change in tooth vitality (the response of the pulp tissue toward external stimuli) | This outcome will be measured one day before the six maxillary anterior teeth retraction initiation (T0) and immediately after the completion of retraction (T1) which is expected to occur in 4 months | Tooth vitality will be evaluated for each tooth of the six maxillary anterior teeth using Ethyl Chloride applied by a cotton roll on each tooth, which will indicate negative response (no vitality) or positive response (vital pulp) |
| Root resorption | A CBCT image will be taken one day before the six maxillary incisors retraction initiation (T0) and immediately after the completion of retraction (T1) which is expected to occur in 4 months | Assessment will be performed by subtracting the root length of each maxillary anterior tooth after retraction from its length before starting retraction procedure. |
| Change in the Oral Health Related Quality of Life associated with anterior teeth retraction. | The OHIP-14 will be assessed immediately after application, after 1, 7, 14, and 28 days of the six maxillary anterior teeth retraction initiation | Assessment will be performed using the OHIP-14 questionnaire; which is a questionnaire that include 14 questions regarding different aspects of problems that might be associated with retraction (discomfort, stress, chewing difficulties, ...). the patient could choose the answer from a five-point Likert scale (Never, Hardly ever, Occasionally, Fairly often, Very often) |
| Changes in the levels of pain and discomfort | These levels will be assessed at: one day, one week, two weeks, and four weeks following the intervention | Assessment will be performed using questionnaires that include Visual Analog Scale (VAS) for each question, the scale has a minimum scale of 0 (no pain or discomfort) and a maximum scale of 100 (maximum pain or discomfort). |
| Maxillary first molar anchorage loss | This outcome will be measured one day before upper incisors' retraction initiation (T0) and immediately after the completion of retraction (T1) which is expected to occur in 4 months | Assessment will be performed on study casts by calculating the amount of mesial drifting of the maxillary molar (if any) in millimeters before and after retraction |
Countries
Syria
Outcome results
None listed