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临床试验/NCT04658446
NCT04658446尚未招募不适用

Comparison Between Augmented Reality-Assisted Bonding Versus Digitally-Assisted Indirect Bonding in Orthodontic Patients (Randomized Clinical Trial)

Seif El-Din Amr Hussein Hegab0 个研究点目标入组 8 人开始时间: 2024年2月25日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
8
主要终点
Patient Convenience

研究概览

简要总结

Comparing two indirect bonding techniques. Augmented Reality-assisted bonding and Digital 3D printed indirect bonding trays in regards to patient convenience, accuracy of bracket placement and time consumption of each technique used.

详细描述

Augmented reality is a relatively new addition to the digital armamentarium. It is becoming increasingly popular especially among surgeons, whether general or dental. In light of the clinicians whom have relied on augmented reality in their fields of work, it was suggested that an augmented reality-assisted orthodontic bonding guide be of use. Such an application would theoretically solve many issues of the indirect bonding techniques at hand.

In this study, we shall investigate whether the theory behind such an augmented reality-assisted bonding guide is on par with the digitally-assisted indirect bonding in terms of patient convenience, accuracy of bracket placement and time consumption of the bonding process, to see whether it qualifies to be a method among all the other methods stated in the literature for indirect bonding.

Digital indirect bonding has many advantages, one of which is achieving greater accuracy in bracket positioning, however it has some down sides such as excess composite flashes around brackets after curing and the cost of 3D printing.

Aim of the Study Is to evaluate the patients' convenience upon using the newly introduced augmented reality-assisted bonding guide in comparison to the digitally-assisted indirect bonding tray. Secondary objectives such as accuracy and procedure time consumption between the two methods are also of importance.

Null Hypothesis There will be no difference in the patients' convenience, accuracy and procedure time consumption between the two methods proposed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Device Feasibility
盲法
Single (Outcomes Assessor)

盲法说明

The assessor shall not know which group is which in the accuracy outcome.

入排标准

年龄范围
15 Years 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Arch length deficiency ≤ 5 mm.
  • Good oral hygiene.
  • Fully erupted permanent dentition, not necessarily including third molars.

排除标准

  • Patient with active periodontal diseases.
  • Anterior cross-bite.
  • Enamel hypoplasia.
  • Previous orthodontic treatment.
  • Teeth with caries or restorations on labial surfaces.

结局指标

主要结局

Patient Convenience

时间窗: Immediately after the bonding procedure.

Whether the patient was at ease during the bonding procedure or not and the overall convenience of the procedure from the patient's point of view.

次要结局

  • Time(At the time of the Bonding Procedure.)
  • Accuracy of the Method(After one week of the Bonding Procedure.)

研究者

发起方
Seif El-Din Amr Hussein Hegab
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Seif El-Din Amr Hussein Hegab

PhD Candidate/ Researcher

Cairo University

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