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Assessment of Treatment Efficacy Using Smile Arc Marginal Ridge Approach Versus MBT Chart Method for Bracket Positioning

Not Applicable
Recruiting
Conditions
Class I Malocclusion
Registration Number
NCT06652230
Lead Sponsor
Cairo University
Brief Summary

The goal of this randomized clinical trial is to evaluate the effect of Smile Arc Marginal Ridge Approach (SAMRA) versus MBT chart method for bracket positioning on orthodontic treatment results.

The main questions it aims to answer are:

Is there a difference in orthodontic treatment results between smile arc marginal ridge approach (SAMRA) and MBT chart method for bracket positioning?

Does SAMRA provide more accurate orthodontic results and reduce the number of archwire bendings and brackets repositioning needed during finishing?

The investigators will compare Smile Arc Marginal Ridge Approach (SAMRA) with MBT Chart Method (gold standard) to see if SAMRA provides more accurate orthodontic results and reduce the need for archwire bendings and brackets repositioning during finishing.

Participants will:

* Undergo orthodontic treatment and divided into two groups, Group A (SAMRA) and Group B (MBT Chart Method).

* 0.018-inch MBT brackets will be used in both groups.

* Follow ups every 1 month will take place to change the archwires after becoming passive.

* After leveling and alignment is completed, orthodontic treatment results, number of archwire bendings and brackets repositioning needed will be determined to see which type of intervention is better or if both provide similar results.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Orthodontic patients aged 11-30 years old.
  • Mild or moderate crowding not requiring tooth extraction.
  • Full permanent dentition including fully erupted 7s not necessarily 8s.
  • Good oral hygiene.
  • Skeletal and dentoalveolar class I malocclusion.
Exclusion Criteria
  • Systemic disease potentially affecting the study outcome.
  • Cleft lip and palate/syndromic patients.
  • Any signs or symptoms of temporomandibular disorders (TMD).
  • Previous orthodontic treatment.
  • Pregnant females.
  • Chronic use of medications.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Orthodontic treatment results6 months

Orthodontic treatment results will be assessed according to the American Board of Orthodontics Objective Grading System (ABO-OGS) using the ABO measuring gauge.

Secondary Outcome Measures
NameTimeMethod
Number of additional archwire bending and bracket repositioning needed6 months

Trial Locations

Locations (1)

Faculty of Dentistry Cairo University

🇪🇬

Cairo, Manial, Egypt

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