Efficiency of Using Copper-Nickel-Titanium Versus Nickel-Titanium Arch Wires on Anterior Segment Crowding Alleviation in Group of Adults With Moderate Crowding

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

2021-03-18

Study Completion Date

2022-04-18

Brief Summary

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Evaluate the efficiency of using copper nickel titanium (CuNiTi) arch wire on the initial stage of leveling and alignment regarding their rate of alignment in comparison to Conventional Nickel Titanium arch wire (NiTi) by Measuring the amount and rate of alignment achieved every 2 weeks for a period of 2 months.

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Detailed Description

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Leveling and alignment is the first stage in fixed orthodontic treatment, performed for every patient. Copper nickel titanium (CuNiTi) was modified from conventional nickel titanium (NiTi) to stabilize the super elasticity properties of the initial nickel titanium (NiTi) arch wire against cyclic deformation. The addition of copper to traditional nickel titanium enhances thermal reactive properties and consistency of forces.so the aim of the study is to Evaluate the efficiency of using copper nickel titanium (CuNiTi) arch wire on the initial stage of leveling and alignment regarding their rate of alignment.

Conditions

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Crowding of Anterior Mandibular Teeth

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Patient will receive 0.014 round Copper Nickel titanium CuNiTi archwire and will be ligated using a ligature wire

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

i) To participant (subjects): Patients can be blinded as they do not know the type of wire used. ii) To Assessor: The assessor (different than the main operator) will carry out the measurements blindly on the pre and post models.

Study Groups

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Nickel titanium NiTi arch wire (Gold Standard, control group)

Patient will receive 0.014 round Nickel titanium NiTi archwire and will be ligated using a ligature wire with Follow up for 2 months.

Group Type OTHER

Copper Nickel titanium arch wire

Intervention Type DEVICE

Patient will receive 0.014 round Copper Nickel titanium CuNiTi archwire and will be ligated using a ligature wire.

Interventions

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Copper Nickel titanium arch wire

Patient will receive 0.014 round Copper Nickel titanium CuNiTi archwire and will be ligated using a ligature wire.

Intervention Type DEVICE

Other Intervention Names

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CuNiTi

Eligibility Criteria

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Inclusion Criteria

1. Adult patients aged (18\~33).
2. Moderate crowding (4-8)10.
3. No extractions required.

Exclusion Criteria

1. Previous orthodontic treatment.
2. Missing teeth other than the wisdoms.
3. Patient with dental anomalies.
4. Patient having a deep bite, open bite or cross bite.

Minimum Eligible Age

18 Years

Maximum Eligible Age

33 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes