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Completed

NCT Number: NCT04383600

Flapless Mops for Acceleration of Canine Retraction

The aim of the present clinical study was directed to evaluate the effectiveness of micro-osteoperforations on the rate of canine retraction; in addition, the potential risk for root resorption during maxillary canine retraction.

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Key information

Age range

14 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Al azhar university

Cairo, Egypt

About this study

The aim of the present clinical study was directed to evaluate the effectiveness of micro-osteoperforations on the rate of canine retraction; in addition, the potential risk for root resorption during maxillary canine retraction.

This study was conducted on a total sample of 24 canines of 12 patients, 8 females and 4 males, with mean age was 16.17 ± 2.29 years old who required therapeutic extraction of maxillary 1st premolars and canine retraction. They were selected randomly from the Outpatient Clinic, Department of Orthodontics, Faculty of Dental Medicine (Boys), Al-Azhar University, Cairo, Egypt.

Both maxillary canines, in each patient, were randomly assigned to either an experimental side or the control side in a simple split-mouth design. In the experimental side, micro-osteoperforations was performed distal to the maxillary canine before starting retraction, while the canines in the contralateral control side were retracted without micro-osteoperforations.

Extraction was done at the start of the treatment, and before fitting of the orthodontic appliance. Then upper dental arches were leveled and aligned using conventional sequences of wires.

Three flapless micro-osteoperforations was performed by using orthodontic miniscrews distal to the maxillary canines in the experimental side before starting retraction. Each perforation was 1.6 mm in diameter and 3-4 mm depth into the bone. Canines were completely retracted on 0.016 × 0.022 ̋ stainless steel wires by using closed coil spring delivered 150 gm force.

Patients were followed up every 28 days until complete canine retraction. Routine orthodontic records were obtained for each patient before treatment.

Additionally, a full skull CBCT images were taken before treatment and immediately after canine retraction.

The rate of canine retraction was assessed clinically; in addition, cone beam CT (CBCT) scans were used to assess the amount of canine retraction root length changes. Also anchorage loss of first permanent molars were assessed.

The treatment results were compared clinically and radiographically (CBCT).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • An age ranged between 14 to 18 years.
  • Class II division 1 malocclusion or Class I bimaxillary protrusion with mild or no crowding. Wherever crowding was present, it was symmetrical on both sides of the arch.
  • Patients who diagnosed to require extraction of at least maxillary first premolars bilaterally as a part of their treatment plan.
  • Complete permanent dentition (3rdmolars were not included).
  • Good oral and general health.
  • No history of periodontal problems.
  • No therapeutic intervention planned involving intermaxillary or other intraoral or extraoral appliances during the study period.

Exclusion criteria

  • Blocked out or impacted maxillary canines.
  • Transverse and/or vertical skeletal dysplasia or craniofacial anomalies.
  • Systemic diseases or regular use of medications that could interfere with orthodontic treatment.
  • Previous orthodontic treatment.

Treatment and study plan

micro-osteoperforation

Procedure

three flapless micro-osteoperforations was performed distal to the maxillary canine before starting retraction.

Other names: Mops

Primary outcomes

  1. Rate of canine retraction

    Time frame: change from start of canine retraction until complete space closure up to 6 months

    Clinically, patients were evaluated immediately before canine retraction and every 4 weeks till complete space closure (complete canine retraction).

    It was based on measuring the distance between the contact points on the distal surface of the canines and the contact points on mesial surface of the second premolars.

  2. Canine root length changes

    Time frame: change from start of orthodontic treatment until complete space closure up to 9 months

    The CBCT scans were taken before orthodontic treatment and after complete space closure (canine retraction) to be analyzed for assessment of Canine root length changes.

    The root length was measured along the axis of the root, perpendicular to a line connecting the buccal and palatal cemento-enamel junction CEJ in sagittal view

Secondary outcomes

  1. Anchorage loss of maxillary first permanent molars.

    Time frame: change from start of orthodontic treatment until complete space closure up to 9 months

    mesial movement of maxillary first permanent molars bilaterally was measured before orthodontic treatment and after complete space closure ( canine retraction) on CBCT scan which were taken before orthodontic treatment and after complete canine retraction The distance measured along perpendicular from distal surface of 1st permanent molar to Ptv plane

Sponsors and collaborators

Lead sponsor

Ahmed Akram Elawady

Other

Registry information

Official study title

Efficacy of Micro-osteoperforations on the Rate of Maxillary Canine Retraction: A Randomized Controlled Trial

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
May 12, 2020
Registry last updated
May 12, 2020

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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