Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12615000593538
Ethics application status
Approved
Date submitted
26/05/2015
Date registered
5/06/2015
Date last updated
6/06/2016
Type of registration
Prospectively registered

Titles & IDs
Public title
The effects of micro-osteoperforations on orthodontic root resorption and tooth movement - A pilot study
Scientific title
The effect of micro-osteoperforations into the alveolar bone versus no micro-osteopeforations on root root resorption and rate of tooth movement in patients who require upper premolar extractions as part of their overall orthodontic treatment plan
Secondary ID [1] 286816 0
nil known
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
orthodontic root resorption
 295187 0
Condition category
Condition code
Oral and Gastrointestinal 295437 295437 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The study involves participants who require upper premolar extractions as part of their overall orthodontic treatment plan.
First part:
The first part of the project involves placing orthodontic braces only on the upper posterior teeth. Using a split-mouth design, one side will be randomly made control, while the other will be the experimental side in which micro-osteoperforations will be placed. Micro-osteoperforations involves the placement of a series of small punctures through the gingiva and alveolar bone associated with the roots of teeth to stimulate a localized inflammatory process. A specialized instrument designed specifically for micro-osteoperforations will be used.
Three perforations 3-7mm deep in a vertical alignment will be placed on both the mesial and distal aspects of the upper first premolar. Including the anaesthetic administration, the micro-osteoperforation procedure would take approximately 30 minutes.
Using partial braces on the upper posterior teeth (first and second premolar and first molar), orthodontic force will be applied to the first premolars bilaterally for 4 weeks, after which the teeth will be extracted as part of the patient’s ongoing orthodontic treatment. These extracted teeth will then be scanned with a MicroCT scanner and the extent of resorption measured. Patients will also be asked to record their level of discomfort on the experimental and control side following the placement of braces and micro-osteoperforations.
Second part:

The second part of the study involves placing full braces on the subjects. This will take place around 2 weeks after the extractions of the premolars and conclusion of the first part of the study. It will involve 24 weeks of aligning and levelling teeth. After this period, another three perforations in a vertical alignment will be placed distal to the upper canine on the experimental side and the rate of canine retraction will be compared to the control side. Patients will be assessed and tooth movement measured off study models every 2-4 weeks, over an 8-week period.
Intervention code [1] 291974 0
Treatment: Surgery
Intervention code [2] 292003 0
Treatment: Devices
Comparator / control treatment
The control would be the randomly selected side of the mouth where there will be no micro-osteoperforations.
First part:
Like the intervention side, an orthodontic force will be placed to move the upper first premolar buccally (towards the cheek) for 4 weeks, after which the premolar would be extracted and examined under Micro-CT to assess extent of root resorption. Second part:
The rate of orthodontic space closure of the first premolar extraction space at the control side would also compared with the intervention side.
Control group
Active

Outcomes
Primary outcome [1] 295170 0
Amount of orthodontic root resorption. The premolar roots will be scanned with a MicroCT scanner and the extent of root resorption measured.
Timepoint [1] 295170 0
4 weeks post orthodontic forces
Secondary outcome [1] 314940 0
Orthodontic tooth movement. This will be measured clinically inside the mouth every 2 weeks for 8 weeks, and also from models from impressions of the teeth.
Timepoint [1] 314940 0
32 weeks after commencement of orthodontic treatment

Eligibility
Key inclusion criteria
Need for bilateral maxillary first premolar extractions (necessitating moderate anchorage requirements) and fixed appliance treatment;
Permanent Dentition;
Apexification (root formation) completed;
Similar degree of minimal crowding on each side of the maxillary arch
Minimum age
12 Years
Maximum age
18 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Previous orthodontic or orthopaedic treatment;
Craniofacial anomaly present;
Previous reported or observed dental treatment of the maxillary canines;
History of trauma, bruxism or parafunction;
Past and present signs and symptoms of periodontal disease;
Significant medical history or medication that would adversely affect the development or structure of the teeth and jaws and any subsequent tooth movement.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Patients will be recruited from the orthodontic waiting list at Sydney Dental Hospital.
The Orthodontic Department routinely screens patients to assess whether they have an orthodontic problem that requires treatment. The patient is placed on the appropriate waiting list if the quality for treatment.
Patients with a specific orthodontic problem (maxillary protrusion or bimaxillary protrusive and severe crowding) are selected from the waiting list.
These patients are sent a letter from the Head of Department inviting their participation in the study. These patients are asked to attend for an examination to screen for eligibility for the study, if they meet the criteria, they are then invited to participate in the research project.
When interested patients attend for screening, they are asked to complete the Participant Consent Form before any screening procedures are undertaken.
If the patients are ineligible for the study, they will commence their routine clinical care immediately and will not be returned to the waiting list.
Allocation is not concealed due to the split-mouth design of the study (one side of the mouth would be randomly assigned to be experimental and the other side would be assigned as control). However, as the same operator is going to place the micro-osteoperforations and examine the root resorption, the extracted premolars will be given a random de-identification number which will be stored on master spread sheet. This will be done to prevent the operator from knowing which tooth was experimental or control.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Sides of mouth would be randomly assigned as experimental or control via coin toss (heads and tails allocated as right and left).
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?


The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
20/07/2015
Actual
1/10/2015
Date of last participant enrolment
Anticipated
30/06/2016
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
15
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 3844 0
Sydney Dental Hospital - Surry Hills

Funding & Sponsors
Funding source category [1] 291358 0
Hospital
Name [1] 291358 0
Department of Orthodontics, Sydney Dental Hospital
Country [1] 291358 0
Australia
Primary sponsor type
Charities/Societies/Foundations
Name
Australian Society of Orthodontics Foundation for Research and Education
Address
Level 3, 33-35 Atchison Street
St Leonards NSW 2065
Country
Australia
Secondary sponsor category [1] 290037 0
Commercial sector/Industry
Name [1] 290037 0
Pacific Orthodontics
Address [1] 290037 0
Pacific Orthodontics Pty Ltd
P.O. Box 885
Kenmore, Brisbane
QLD 4069
AUSTRALIA
Country [1] 290037 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 292919 0
SLHD Ethics Review Committee (RPAH Zone)
Ethics committee address [1] 292919 0
Ethics committee country [1] 292919 0
Australia
Date submitted for ethics approval [1] 292919 0
26/05/2015
Approval date [1] 292919 0
14/08/2015
Ethics approval number [1] 292919 0
EC00113

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes
Attachments [1] 469 469 0 0
/AnzctrAttachments/368641-Microosteoperforations ethics application.doc
Attachments [2] 470 470 0 0
/AnzctrAttachments/368641-RESEARCH PROTOCOL.docx

Contacts
Principal investigator
Name 57622 0
Prof M. Ali Darendeliler
Address 57622 0
Sydney Dental Hospital
2 Chalmers St
Surry Hills NSW 2010
Country 57622 0
Australia
Phone 57622 0
+612 9351 8314
Fax 57622 0
Email 57622 0
[email protected]
Contact person for public queries
Name 57623 0
Emmanuel Chan
Address 57623 0
Sydney Dental Hospital
2 Chalmers St
Surry Hills NSW 2010
Country 57623 0
Australia
Phone 57623 0
+612 9351 8314
Fax 57623 0
Email 57623 0
[email protected]
Contact person for scientific queries
Name 57624 0
Emmanuel Chan
Address 57624 0
Sydney Dental Hospital
2 Chalmers St
Surry Hills NSW 2010
Country 57624 0
Australia
Phone 57624 0
+612 9351 8314
Fax 57624 0
Email 57624 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseEffectiveness of minimally invasive surgical procedures in the acceleration of tooth movement: a systematic review and meta-analysis.2016https://dx.doi.org/10.1186/s40510-016-0146-9
N.B. These documents automatically identified may not have been verified by the study sponsor.