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Completed

NCT Number: NCT04020952

Effect of Archwire Gauge on the Rate of Canine Retraction

trial will be done to evaluate the effect of archwire gauge on the rate of canine retraction, canine tip and torque, root resorption and loss of anchorage in maxillary dental protrusion cases requiring first premolars extraction.

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Key information

Conditions

Age range

16 year–26 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

faculty of dentistry, Cairo University

Cairo, Egypt

About this study

Three working archwires of different gauges will be used during canine retraction; st.st 0.019×0.025" as a comparator, st.st 0.016×0.022" and st.st 0.017×0.025" wires as interventions. after levelling and alignment till reaching the working archwire, it will be left in place for a month then maxillary first premolars will be extracted and base line records will be taken(digital models, digital periapical radiographs and panorama). digital models will be taken monthly to measure rate of canine retraction for 6 months. after 6 month evaluation of anchorage loss, change in canine tip and torque will be done on last obtained digital model , panorama will be taken to evaluate the change in canine tip and digital periapical radiograph will be taken and compared with the preretraction radiograph to evaluate amount of root resorption.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult females (age range 18-28 years old).
  • Maxillary dental protrusion indicating first premolars extraction.
  • Full permanent dentition (not necessitating third molars).

Exclusion criteria

  • Patients having systemic diseases or on medications that would affect tooth movement.
  • Active periodontal disease or obvious bone resorption in maxillary arch.
  • Patients with habits that are detrimental to dental occlusion (thumb sucking, tongue thrusting … etc.).
  • Previous orthodontic treatment.
  • Missing teeth.

Treatment and study plan

st.st 0.019×0.025" wire

Other

rectangular stainless steel wire that will be used during canine retraction after first premolars extraction

st.st 0.016×0.022" wire

Other

rectangular stainless steel wire that will be used during canine retraction after first premolars extraction

st.st 0.017×0.025" wire

Other

rectangular stainless steel wire that will be used during canine retraction after first premolars extraction

Primary outcomes

  1. rate of canine retraction

    Time frame: 6 months

    the distance that canine moved every month

Secondary outcomes

  1. change in canine tip

    Time frame: 6 months

    change in canine crown tipping to certain reference plane with the aid of cone beam computed tomography

  2. change in canine torque

    Time frame: 6 months

    change in canine crown and root torque to certain reference plane with the aid of cone beam computed tomography

  3. loss of molar anchorage

    Time frame: 6 months

    assess from digital models if there is change in mesio-distal position of maxillary first molar

  4. amount of canine root resorption

    Time frame: 6 months

    assess amount of root resorption (if occurred) with the aid of cone beam computed tomography

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Effect of Archwire Gauge on the Rate of Canine Retraction in Adults: A Randomized Clinical Trial

Important dates

Study start
2019
Primary completion
2020
Study completion
2021
First posted
Jul 16, 2019
Registry last updated
Jul 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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