Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT05818527 |
| Other study ID # |
tooth acceleration |
| Secondary ID |
|
| Status |
Completed |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
September 2015 |
| Est. completion date |
September 2017 |
Study information
| Verified date |
July 2023 |
| Source |
Cairo University |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
The goal of this Randomized controlled clinical trial is To investigate the effectiveness of
AcceleDent Aura vibrating device on rate of canine retraction in orthodontic treatment.. The
main question[s] it aims to answer are:
• 1st question In Patients with class II requiring canine retraction it possible to
accelerate canine retraction safely using AcceleDent? 2nd question: is accelerating teeth
movement effect root condition ? the study will be done on Orthodontic patients with class II
requiring canine retraction Excluding Any dental or medical disease affecting tooth movement.
Description:
Introduction:
orthodontic tooth movement(OTM) is a process of mechanically-induced bone modeling where new
bone is formed on the tension side and resorbation on the compression side of the periodontal
ligament.
One of negative points of orthodontic treatment is long time treatment (24 month ).
Accelerating the speed of orthodontic tooth movement should contribute to the shortening of
the treatment period Many approaches was used such as approaches with low-energy laser
irradiation and magnetic fields as well as pharmacological approaches with the injection of
prostaglandin E2 (PGE2) and However, many side effects, such as local pain, severe root
resorption and drug-induced side effects have been reported.
A new device called AcceleDent(OrthoAccel technologies,Inc, USA) has been introduced to the
market and aims to achieve an increased rate of tooth movement by enhancing bone remodelling
using pulsating forces. Invented by Dr. Jeremy Mao, it is intended to be used by a patient in
conjunction with fixed orthodontic appliances or removable sequential aligner treatment for
20 mins per day. It vibrates at a frequency of 30Hz and has force amplitude of 20 grams.
It was found in kau et al ( split mouth study trial) in that the total rate of movement for
the mandibular crowding was 2.1 mm per month and for the maxillary arch was 3.0 mm per month,
which apparently is faster than the traditional finding as of about 1.0 mm per month . The
patient compliance was 67% with good patient perception. It was thus concluded that the
AcceleDent device is a useful adjunct to orthodontic treatment.
The prolonged time of orthodontic treatment especially during extraction cases requiring
canine retraction become a major challenge which have not been solved in clinical
orthodontic, solving this challenge using AcceleDent will decrease the treatment time of
canine retraction thus improve the quality of orthodontic care and improve patient
compliance.
Our aim is evaluating the efficiency of device in accelerating tooth movement and shorting
time of canine retraction.
Research Hypothesis:
The vibratory stimulation using AcceleDent can accelerate canine retraction, Animal studies
have shown that the application of cyclical forces in conjunction with an orthodontic force
could increase the rate of orthodontic tooth movement by enhancing bone remodeling activity .
PICOS P- Patients with class II requiring canine retraction I- accelerating canine retraction
using AcceleDent C Patients with class II requiring canine retraction using nickel titanium
closed spring without AcceleDent O 1ry rate of canine retraction in mm per month. 2ry assist
inflammatory root resorption using root resorption index.
Trial design:
Randomized controlled trial
Study setting:
The study will be performed in the outpatient clinic of the Orthodontic Department at the
Faculty of Oral and Dental Medicine, Cairo University
Eligibility Criteria:
- Subjects will be on the following inclusion criteria:
1. Complete permanent dentition
2. Class II malocclusion that needs first premolar extraction and canine retraction
3. Subjects with clinically acceptable oral hygiene ( probing depth not exceed 3mm)
- Subjects will be excluded from the study if the following conditions existed:
1. Any medical could impact study results during the expected length of the study.
2. Subject was currently using any investigational drug that influence tooth movement
(Bisphosphonates, Acetaminophen)15 or any other investigational device.
3. Subject had plans to relocate or move within 6 months of enrollment.
Intervention:
1. All the patients who will met inclusion and exclusion criteria will be randomly assigned
into 2 groups; control and experimental group.
2. For each patient, MBT prescription preadjusted brackets with 0.022*0.025 inch slot (3m
Gemini metal brackets, 3m Unitek Corporation, Monrovia, A, USA) will be bonded on the
teeth after the first premolars extraction by (T.I)
3. For anchorage preparation, TADs will be used(it will be placed between mesil upper first
On the sides requiring anchorage supplementation,1.6-mm TADs (American Orthodontic,US)
were placed under local anesthesia, usually at the junction of the attached gingivae
with the reflected mucosa and mesially to the maxillary molars. The TADs will be placed
before any retraction force placed on the canines16 by (T.I).
4. The canine retraction will be done using Ni-Ti closing spring (3m Unitek Corporation,
Monrovia, A, USA),150 gms of force will be used17.
5. The experimental group will be instructed for using AcceleDent from the time of starting
canine retraction for 20 mins/day.
6. An alginate impression for the upper arch will be taken monthly. The plaster models will
be collected (T0-T4) were digitized using desktop scanner (3Shape R500, 3shape,
Copenhagen, Denmark) The canine retraction was assessed using two methods; the
incremental rate of canine retraction and the total distance travelled by the canine.
Using the 3Shape OrthoAnalyzer software‡ the four consecutive models (T1-T4) were
superimposed9 on the base model (T0) using three points registration upon the third
rugae area . Colour-mapped superimposition was used to verify the accuracy of the
superimposition. The difference in the position of the canine cusp tip was used to
calculate the incremental rate of canine retraction (Figure 3). For intra- and
inter-rater reliability, measurements of the digital models will done by the same
operator (NA) twice, 2 weeks apart and repeated by another operator (MA).
.Measurements of the total distance of canine retraction, the canine tipping, torque and
rotation were analysed by measuring the angles between the long axis lines for the canines
and the three reference planes were measured to detect tipping and torque movements. Also,
the angle between the horizontal line of the first molar and the sagittal plane to detect
canine rotation.
For assessment of root resorption, the axial guided navigation method explained by Castro et
al10 and Schwartz et al11 was used. Using the software In-vivo , version 5.3(Anatomage, Inc.,
Santa Clara, CA 95054, USA). the pre- & post-retraction CBCTs obtained for each patient were
used to evaluate the effect of AcceleDent on root resorption, the linear length between the
root apex and cusps tip was measured.
The evaluation was carried by two blinded examiners. In order to fully visualize the root,
the CBCT image was re-oriented on each root so that the cross-section would pass through the
long axis of each canine .
The degree of pain was measured by Visual Analog Score (VAS), these charts were filled by the
patients for the following week after beginning of canine retraction at time intervals (0, 24
hours , 48 hours, 72 hours and 7 days ) and were gathered at the end of the week. The pain
VAS was in the format of a chart that contained a series of 10-cm horizontal scales on which
the patient marked the degree of pain (0 to 10, where 0 refer to no pain and 10 refer to
sever pain) at the indicated time periods.
Criteria for discontinuing or modifying the allocated intervention:
Patient who had active peridontitis or loss of any of permanent tooth (except third molar) or
dental trauma or failure of bonding on maxillary canine during experiment will have to stop
the trial.
Adherence:
The patients will be asked to attend regular follow up visits and their adherence to the
appointments will be regularly monitored. The patient adherence to intervention instruction (
to use the appliance 20 mins/day) will be monitored by asking the patient and writing every
day on chart how long he/she used it?
Outcomes:
Out come Measurement
1. ry Canine retraction mm per month
2. ry Root resorption R.R index
Participant timeline:
Visit Treatment Models CBCT
1. Initial records Yes Yes
2. Brackets and wire placement after premolar extraction Yes No
T0 Start canine retraction In experimental group start the use of acceledent Yes N o 4 T1 1
month after retraction Yes No 5 T2 2 month after retraction Yes No 6 T3 3 month after
retraction Yes No 7 T4 4 month after retraction Yes No 8 T5 5 month after retraction Yes No 9
T6 6 month after retraction Yes Yes
Sample size calculation The aim of the study is to evaluate the efficiency of using vibrating
device (AcceleDent) in accelerating canine retraction. Based on previous studies the outcome
variable is normally distributed and an expected effect size of approximately 0.8. A total
sample size of 52 canines will be sufficient to detect a large effect size (d=0.8) estimated
from published paper by Kau et al., with power 80% and 5% significance level. This number has
been increased to a total sample size of 64 canines (32 in each of the two groups) to allow
for losses of around 25% during follow up.
Sample size was calculated using G*Power program, University of Düsseldorf, Düsseldorf,
Germany (Faul, F., et.al.).
Statistical methods:
Data management and Statistical analysis will be done using Statistical Package for Social
Sciences, Version 21.0 (SPSS, IBM) for Windows. Canine retraction in mm will be presented as
mean and standard deviation (SD) or median and range, as appropriate. Percentages will be
calculated for inflammatory root resorption.
Differences between continuous variables will be done by Student's t test or Mann-Whitney
U-test variables as appropriate. The differences between percentages will be tested using the
Chi square test or Fisher's exact test, as appropriate.
P-value <0.05 will be considered statistically significant. All tests will be two-sided.
Allocation:
Sequence generation:
Patients will be randomly assigned to group A (treatment) or B (control) using computer
randomization sequence generation into 1:1 at Random.org
Concealment mechanism:
Using sequentially numbered opaque sealed envelopes after signing the informed consent to be
enrolled in the study. According to the number, the patients will be then allocated into one
of the groups using a randomization table.
Implementation:
The allocation sequence will be generated by a E.Z (Secretary of the orthodontic department)
who is not involved in the study. This will be contacted to implement the allocation Blinding
: ( the operator and assessor will blinded )
- The operator will be blinded from both groups, (M.N) will be responsible for giving the
patient appliance and the follow up of his adherence to instruction
- Only the patients will not be blinded due the nature of the trial
- The assessor (T.F) will be blinded from both the intervention and also the groups
Data collection method:
CBCT ( Siron CBCT, Sirona Dental Systems Inc, New York, USA) and casts
Plans to promote participants retention and complete follow-up:
Telephone numbers of all patients included in the study will be recorded. All patients will
be given reminder phone calls at the time of the predetermined follow up dates.
Data management:
- All data will be entered in the computer at the Orthodontic department.
- Resulted data from CBCT, casts analysis will be organized and stored.
- The patients' data should have sequential numbers that will be revised at each step to
avoid any mixing of data between patients
Harms:
The patient will be informed in the consent about the 2ry outcome that will be assessment of
root resorption , which has not been yet reported in the literature
Interim Analysis:
No interim analysis is to be performed.
Auditing:
The study supervisors will review the trial. The processes to be reviewed will include
participant enrolment, consent, eligibility and allocation to study groups; adherence to
trial interventions and policies to protect participants, including reporting of harms.
Research ethics approval:
This protocol will be reviewed, approved and agreed upon by CEBD [Center For Evidence Based
Dentistry CU] Cairo University, Egypt, and approved by the Ethics Committee [Research Ethics
Committee Cairo University Faculty of Oral and Dental Medicine].
Protocol amendments:
Any modifications to the protocol will be agreed upon by the Orthodontics and Dentofacial
Orthopedics department.
Consent The trial will be explained to the patients. The researcher will discuss the
interventions and possible harms with patients. The researcher will obtain written consent
from the patients' parents willing to participate in the trial.
Confidentiality:
All study-related information will be stored securely at the Orthodontic department. All
participant personal information will be of limited access. Access will be limited to the
minimum number of individuals. All records that contain names will be stored to secure the
blinding of analysis.
Declaration of interests:
No financial conflicts of interests are to be declared. The study is self-funded by the
researchers.
Access to data:
The researcher and supervisors will have access to the final data sets. All data sets will be
password protected. All the data have to be of no access to others until the study is
finished.
Ancillary and post-trial care:
All the patient will complete their treatment at out patient clinic Dissemination policy
Trial results will be available and A copy of the thesis will be available at the faculty
library.
The authors will publish the trial results in angle orthodontics
Funding:
The trial will be self-funded
