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CompletedNCT04887974Updated May 14, 2021

Canine Retraction With Temporary Anchorage Devices

An interventional study of canine retraction in Class II Malocclusion, Class III Malocclusion and Crowding, Tooth, sponsored by Future University in Egypt. Completed at 1 site in Egypt. Open to participants aged 18 Years to 25 Years. Per ClinicalTrials.gov, last updated 2021-05-14.

Sponsored by Future University in Egypt · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 years 1 month after the study started (first participant enrolled Apr 2016, registered May 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years to 25 Years
Sex
All
01

Study summary

Various malocclusions require the extraction of the first premolars and retraction of the canines with the need for maximum anchorage. If the canines are pulled into the extraction space using the molar teeth for support, unwanted tooth movement occurs. This study aims to evaluate the effect of temporary anchorage devices and power arms, which are auxiliary orthodontic appliances in reducing undesirable tooth movements.

Read the detailed description

In orthodontic patients who require overjet correction, increased facial convexity, or relief of severe crowding, dental extraction followed by canine retraction is indicated. In conventional orthodontic treatment, the molars are used for anchorage and reinforced with intra-oral or extra-oral appliances. Although effective, this produces unwanted side effects where the molars move mesially and rotate, taking up some of the extraction space. As the canines move into the extraction space they tip backward requiring further uprighting. Power arms are vertical metal extensions placed in the canine brackets. They direct the force to the center of resistance of the tooth to allow bodily movement and prevent canine tipping. Temporary anchorage devices (TADs) are minimally invasive, small screws, inserted in the jaw bones to act as anchorage units instead of the molars.

This study aims to evaluate the effect of the TADs and power arms on the efficiency of canine retraction including the rate of canine retraction and canine tipping as well as mesial molar drift and rotation.

The null hypothesis is that the use of the power arm and the TADs have no effect on the canine retraction rate.

This study is a single-arm, single-center study. Twenty quadrants in 10 adult patients will be selected from the Orthodontic Outpatient Clinic at the Future University in Egypt.

Orthodontic records will be collected including study models, intra- and extra-oral photographs and cone beam computed tomograms.

Molars will be banded and Roth 0.22" brackets will be bonded to the canine and second premolars. Power arms, 8mmin length, will be inserted in the vertical slots of the canine brackets.

The dental arches will be leveled and aligned using consecutive archwires. TADs will be inserted between the second premolars and first molars. The first premolars will then be extracted and canines will be retracted within a week. Canines will be retracted along 0.016" X 0.22" stainless steel archwires using 150 g of force applied by an elastomeric chain. The elastic chain will be replaced every 4 weeks.

After 6 months of canine retraction, the orthodontic records will be collected for comparison.

02

Conditions studied

  • Class II Malocclusion
  • Class III Malocclusion
  • Crowding, Tooth
  • Bimaxillary Protrusion
03

In context

Malocclusion, Angle Class III

57 studies on the registry are indexed under Malocclusion, Angle Class III; 11 are open to participants now.

This study's enrollment of 10 is below the median of 32 across 53 interventional studies indexed under Malocclusion, Angle Class III.

Browse Malocclusion, Angle Class III studies →

Lead sponsor

Future University in Egypt is the lead sponsor of 104 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult orthodontic patient
  • Any malocclusion requiring the extraction of the first premolar and canine retraction
  • Full permanent dentition with the exception of the wisdom teeth.

Exclusion criteria

Exclusion Criteria:

  • Any missing permanent tooth
  • Previous orthodontic treatment
  • Periodontal disease; pregnancy
  • Systemic disease or medication that affects bone metabolism
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (actual)

Study arms

  • Experimental
    Canine retraction

    The canines will be retracted by extending short silver elastomeric chains between the power arms in the canine brackets and the TADs. The applied force will be checked and adjusted to 150 g.

    Procedure: canine retraction

Interventions

  • Procedurecanine retraction

    Canine retraction using elastomeric chains activated every 4 weeks, using power arms to direct force through the center of resistance and TADs for direct anchorage.

06

What researchers measure

Primary outcomes

  1. Canine retraction

    Amount of canine movement in millimeters measured on digital models. . The change in the vertical distance from the canine cusp tip to a line connecting the medial points of the third palatal rugae

    Time frame: Baseline to 6 months

  2. Molar mesial drift

    Amount of molar movement in millimeters measured on digital models. The change in the vertical distance from the mesiobuccal cusp tip to a line connecting the medial points of the third palatal rugae

    Time frame: Baseline to 6 months

Secondary outcomes

  1. Canine tipping

    The change in the angle between the canine long axis, from cusp tip to root apex, and the palatal plane (a plane passing through the incisive foramen and the anterior and posterior nasal spines); measued on the cone beam computed tomogram.

    Time frame: Baseline to 6 months

  2. molar rotation

    The change in the angle between the molar horizontal axis and frontal Plane on the cone beam computed tomogram, in the axial view.

    Time frame: Baseline to 6 months

07

Study locations

1 site
  • Faculty of Oral & Dental Medicine
    Cairo, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 14, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04887974
Responsible party
Yehya Mostafa (Head of the Orthodontic Department, Future University in Egypt) — Principal investigator
First posted
May 14, 2021
Start date
Apr 2, 2016
Primary completion
Jan 14, 2017
Completion
Jan 14, 2017
Last update
May 14, 2021

Study contacts

Yehya Mostafa
study director · Future University in Egypt

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2021. You cannot join it, but the record below documents what was studied.

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