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Enrolling by invitationNCT07879066BMU/2026/8506Updated Oct 16, 2026

Evaluation of Corticotomy-Assisted Canine Retraction Rate

An interventional study of Experimental: Corticotomy¬-Assisted Canine Retraction and Active Comparator / Control: Conventional Canine Retraction in Malocclusion, Corticotomy and Canine Retraction, sponsored by Tanzila Rafique. Enrolling by invitation at 1 site in Bangladesh. Open to participants aged 16 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by Tanzila Rafique · Not applicable, Interventional, and Treatment

Updated Oct 16, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
16 Years to 25 Years
Sex
All
01

Study summary

The goal of this split-mouth randomized clinical trial is to evaluate the effectiveness of corticotomy on maxillary canine retraction rate compared to conventional orthodontic techniques. Each participant acts as their own control. After bilateral maxillary first premolar extractions, one quadrant is randomly assigned to receive corticotomy before retraction, while the contralateral quadrant undergoes standard orthodontic retraction without corticotomy.

Read the detailed description

The goal of this split-mouth randomized clinical trial is to evaluate the effectiveness of corticotomy on maxillary canine retraction rate compared to conventional orthodontic techniques. The main question it aims to answer is Does corticotomy-assisted canine retraction accelerate the rate of tooth movement compared to conventional canine retraction methods? Researchers will evaluate the rate of canine retraction, root resorption, bone density, and pocket depth after corticotomy during the canine retraction phase.

Participants will:

  • Receive fixed orthodontic treatment using a pre-adjusted edgewise appliance system (Roth, 0.018-inch slot).
  • Undergo bilateral maxillary first premolar extractions indicated for orthodontic space closure.
  • Undergo a corticotomy (vertical buccal cortical plate cuts distal to the canine root) at the extraction appointment on one randomly assigned maxillary side (Experimental side).
  • Receive conventional canine retraction with no corticotomy on the contralateral maxillary side (Control side).
  • Have titanium mini-implants (Vector TAS, 1.4 × 8.0 mm) placed bilaterally between the second premolar and first molar for anchorage.
  • Undergo bilateral canine retraction initiated with standardized force (150 gm elastomeric power chain) on a rigid 0.016 × 0.022-inch stainless steel working archwire.
  • Be evaluated at baseline and every 3 months over a 6-month follow-up period to measure canine retraction rate, root resorption, and bone density via CBCT.
02

Conditions studied

  • Malocclusion
  • Corticotomy
  • Canine Retraction
  • Orthodontic Tooth Movement
  • Split-mouth Design
  • Bilateral Maxillary 1st Premolar Extraction

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Keywords

  • Corticotomy
  • Canine retraction
  • Accelerating tooth movement
  • regional acceleratory phenomenon (RAP)
03

In context

Malocclusion

469 studies on the registry are indexed under Malocclusion; 91 are open to participants now.

This study's planned enrollment of 24 is below the median of 36 across 383 interventional studies indexed under Malocclusion.

Browse Malocclusion studies →

Lead sponsor

Tanzila Rafique is the lead sponsor of 5 studies on the registry; 5 are open to participants now.

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

04

Who can participate

Ages eligible
16 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

  • Participants who need both maxillary first molar extractions for orthodontic treatment.
  • Class Ⅰ (Bimaxillary proclination), Class Ⅱ division 1 malocclusion.
  • Participants with full permanent dentition present (excluding 3rd molar).
  • Participants with good general health conditions and oral hygiene status.
  • The age range of the patients will be 16 years to 25 years.
  • Sex of the participants will be male, female, or third gender.
  • The treatment plan of maximum anchorage value preservation used mini-implant anchorage during retraction of teeth to obtain good esthetics and correct the molar relationship.
  • No previous orthodontic treatment.

Exclusion criteria

Exclusion Criteria:

  • Medically compromised patients with uncontrolled diabetes mellitus and compromised immune systems.
  • Participants taking medications that alter bone metabolism like bisphosphonates, nonsteroidal anti-inflammatory drugs (NSAIDs), and on long-term corticosteroids.
  • Vitamin D deficiency.
  • Cleft lip /palate, craniofacial syndrome or facial asymmetry.
  • Severe class Ⅲ malocclusion.
  • Pregnant women.
  • Smoker.
  • Non-compliant patient.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    Experimental: Corticotomy¬-Assisted Canine Retraction

    Corticotomy will be performed on one maxillary quadrant before initiating standardized canine distalization.

    Procedure: Experimental: Corticotomy¬-Assisted Canine Retraction · Procedure: Active Comparator / Control: Conventional Canine Retraction

  • Active comparator
    Active Comparator / Control: Conventional Canine Retraction

    Conventional canine retraction will be performed on the contralateral quadrant without corticotomy under identical orthodontic mechanics.

    Procedure: Experimental: Corticotomy¬-Assisted Canine Retraction · Procedure: Active Comparator / Control: Conventional Canine Retraction

Interventions

  • ProcedureExperimental: Corticotomy¬-Assisted Canine Retraction

    Corticotomy will be performed on one maxillary quadrant before initiating standardized canine distalization.

  • ProcedureActive Comparator / Control: Conventional Canine Retraction

    Conventional canine retraction will be performed on the contralateral quadrant without corticotomy under identical orthodontic mechanics.

06

What researchers measure

Primary outcomes

  1. Rate of maxillary canine retraction

    Linear distal movement of the maxillary canine measured on CBCT scans relative to a fixed anatomical landmark (e.g., the cusp tip, the center of the tooth (midpoint of the line joining the cusp tip and root apex), and the root apex) to compare the corticotomy-assisted side with the conventional side.

    Time frame: 6 months

Secondary outcomes

  1. Overall rate of maxillary canine retraction

    * A frontal reference plane (FP) was constructed to the mid-sagittal and horizontal planes, passing through the incisive foramen and the long axis of the canine. * Three landmarks identified on each CBCT volume: the cusp tip, the center of the tooth, and the root apex. * The perpendicular distance from each of these three landmarks to the FP measured at both experimental and control sides. * The amount of retraction at the cusp tip, center, and root apex calculated as the difference in distdistance-to-FP between successive time point and across the full retraction period.

    Time frame: Baseline to Post-retraction (6months)

  2. Comparison of amount of canine root resorption between the corticotomy- assisted side and the conventional side.

    -Root resorption was calculated (in mm) as the difference in canine length, from cusp tip to root apex, between the pre- and post-retraction CBCTs.

    Time frame: Baseline to Post-retraction (6months)

  3. The rate of retraction at each landmark

    The rate of retraction at each landmark was calculated by dividing the amount of movement by the time elapsed (mm per month).

    Time frame: Baseline to Post-retraction (6months)

  4. Measurement of bone density between the corticotomy-assisted side and the conventional side.

    Bone density was measured between the corticotomy-assisted side and the conventional side over six months by sequential CBCT scans(with the same field of view and the same voxel resolution) taken at T0 (baseline), T1 (3 months), and T2 (6 months).

    Time frame: Baseline to Post-retraction (6months)

  5. Measurement and comparison of the pocket depth of the canine(in mm) between the corticotomy-assisted and the conventional side.

    Pocket depth of the canine was measured between the corticotomy-assisted side and the conventional side by periodontal probing at T0 (baseline), T1 (3 months), and T2 (6 months).

    Time frame: Baseline to Post-retraction (6months)

07

Study locations

1 site
  • Bangladesh Medical University (BMU), Dhaka,1000
    Dhaka, Bangladesh 1000, Bangladesh
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07879066
Lead sponsor
Tanzila Rafique
Responsible party
Tanzila Rafique (Associate Professor, Bangladesh Medical University) — Sponsor-investigator
First posted
Oct 16, 2026
Start date
Aug 8, 2026
Primary completion
Aug 8, 2027 (estimated)
Completion
Aug 8, 2027 (estimated)
Last update
Oct 16, 2026

Study contacts

Mahmood Sajedeen, BDS,FCPS
study director · Bangladesh Medical University (BMU)

Oversight

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

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