Comparison Between the Effectiveness of Different Commercial Bracket Brands

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-01

Study Completion Date

2022-12-01

Brief Summary

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There's a scarcity in literature concerning the comparison of the effectiveness of brackets in its torque and tip ability, the time takes for leveling and alignment comparing between different orthodontic bracket brands, and its effect on the rate of tooth movement. The purpose of this study is to determine, In orthodontic patients with Class I molar relation and teeth crowding, in which different bracket brands will be compared.

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Detailed Description

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Bracket effectiveness can be measured in a variety of ways, including torque, tip, time required for levelling and alignment, bracket failure, and the patient's visual analogue scale. All are viable options; therefore, we want to complete the orthodontic treatment and determine which brackets fulfilled the built-in bracket prescription and achieved success in terms of aesthetics, better smiles, better patient judgement, and function.

Conditions

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Crowding, Tooth, Class I

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Single (Outcomes Assessor) Only the outcome assessors will be blind. The patients name will be sealed from pre and post radiographs and study models. Then two assessors will carry out, blindly and independently, the measurements and analysis of the study

Study Groups

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American orthodontics brackets

Roth prescription, 0.022" slot size

Group Type ACTIVE_COMPARATOR

Brackets

Intervention Type OTHER

Levelling and alignment for the bonded teeth through following the wire sequence: 0.014 NiTi, 16 NiTi, 0.016×0.022 NiTi and 0.017×0.025 StSt. (Wires from American Orthodontics)

• After levelling and aligning is completed the patient will be referred for the uptake of post intervention records; a standardized dental photograph and CBCT after 6- 9 months)

FANTA brackets

Roth prescription, 0.022" slot size

Group Type ACTIVE_COMPARATOR

Brackets

Intervention Type OTHER

Levelling and alignment for the bonded teeth through following the wire sequence: 0.014 NiTi, 16 NiTi, 0.016×0.022 NiTi and 0.017×0.025 StSt. (Wires from American Orthodontics)

• After levelling and aligning is completed the patient will be referred for the uptake of post intervention records; a standardized dental photograph and CBCT after 6- 9 months)

MATT brackets

Roth prescription, 0.022" slot size

Group Type ACTIVE_COMPARATOR

Brackets

Intervention Type OTHER

Levelling and alignment for the bonded teeth through following the wire sequence: 0.014 NiTi, 16 NiTi, 0.016×0.022 NiTi and 0.017×0.025 StSt. (Wires from American Orthodontics)

• After levelling and aligning is completed the patient will be referred for the uptake of post intervention records; a standardized dental photograph and CBCT after 6- 9 months)

Interventions

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Brackets

Levelling and alignment for the bonded teeth through following the wire sequence: 0.014 NiTi, 16 NiTi, 0.016×0.022 NiTi and 0.017×0.025 StSt. (Wires from American Orthodontics)

• After levelling and aligning is completed the patient will be referred for the uptake of post intervention records; a standardized dental photograph and CBCT after 6- 9 months)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient with full set of permanent teeth
* Male and female (14-19 years old).
* Positive patients' acceptance for the study
* Patients have no history of previous orthodontic treatment.

Exclusion Criteria

* Patients with enamel or dentin defect or any teeth anomaly will be eliminated.
* Patients having canine or lateral incisors peg shaped will be excluded from the research. - Medically compromised patients
* Patients unable to give an informed consent
* Patient with periodontal disease
* Patient taking long term medication
* Patients with any parafunctional habits (i.e. Bruxism, tongue thrusting, mouth Breathing)

Minimum Eligible Age

14 Years

Maximum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes