Canine Retraction With Temporary Anchorage Devices

Sponsor
Future University in Egypt (Other)
Overall Status
Completed
CT.gov ID
NCT04887974
Collaborator
(none)
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Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: canine retraction
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Canine Retraction Using Power Arms and Temporary Anchorage Devices
Actual Study Start Date :
Apr 2, 2016
Actual Primary Completion Date :
Jan 14, 2017
Actual Study Completion Date :
Jan 14, 2017

Arms and Interventions

Arm Intervention/Treatment
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
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.

Outcome Measures

Primary Outcome Measures

  1. Canine retraction [Baseline to 6 months]

    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

  2. Molar mesial drift [Baseline to 6 months]

    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

Secondary Outcome Measures

  1. Canine tipping [Baseline to 6 months]

    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.

  2. molar rotation [Baseline to 6 months]

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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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:
  • Any missing permanent tooth

  • Previous orthodontic treatment

  • Periodontal disease; pregnancy

  • Systemic disease or medication that affects bone metabolism

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Oral & Dental Medicine Cairo Egypt

Sponsors and Collaborators

  • Future University in Egypt

Investigators

  • Study Director: Yehya Mostafa, Future University in Egypt

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yehya Mostafa, Head of the Orthodontic Department, Future University in Egypt
ClinicalTrials.gov Identifier:
NCT04887974
Other Study ID Numbers:
  • 20153110
First Posted:
May 14, 2021
Last Update Posted:
May 14, 2021
Last Verified:
May 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 14, 2021