Esthetic Impact of Different Minimally Invasive Approaches on Hypomineralized Permanent Anterior Teeth
Esthetic Impact of Different Minimally Invasive Approaches on Hypomineralized Permanent Anterior Teeth: A Randomized Clinical Trial
The aim of the study is to determine the effectiveness of minimally invasive treatments in reducing the visible enamel opacities on permanent anterior teeth in children aged from seven to twelve years with hypomineralized lesions.
A secondary purpose is to evaluate patient satisfaction and the psychosocial impact of the treatment on the esthetic perception of the treated children.
The results of all the research papers about treating enamel discoloration caused by hypomineralization with the ICON system can be accepted as satisfactory. However, not all cases achieved the full aesthetic aim.
Microabrasion is an acid abrasive removal and not the dissolution of enamel stain. It is as a treatment modality for enamel opacities like brown, orange, or yellow enamel spots; and fluorotic white streaks. Esthetic results could be reached when microabrasion followed by a remineralizing agent such as C PP-ACFP.
Null hypothesis, there is no difference between microabrasion followed by a remineralizing agent and resin infiltration treatment regarding clinical effectiveness & patient satisfaction.
研究概览
地位
地位
干预/治疗
干预/治疗
详细说明
Outcomes:
Primary outcome Color enhancement using Clinical photographs (Bhandari, et al., 2019). Secondary outcomes
- Patient satisfaction will be evaluated using Numerical scale (NS), (Figure 1). The participant marked the number that represented their self-assessed satisfaction (Rocha et al., 2020) as shown in Appenxix II.
- Psychosocial impact of the treatment on the esthetic perception of the treated children will be evaluated using The Psychosocial Impact of Dental Aesthetics Questionnaire (PIDAQ) (Klages et al., 2006). Appendix III.
- Reducing teeth hypersensitivity will be evaluated using The Schiff Cold Air Sensitivity Scale (SCASS) (Schiff et al., 1994).
- Adverse and undesirable side effects experienced by the respondents: a) pain in teeth and gums will be evaluated using The Wong-Baker FACES® Pain Rating Scale (Wong et al., 1988). Appendix IV.
- b) bitter taste will be evaluated by asking the child right after treatment. (Athayde et al., 2022).
- Follow up:
Follow up after 1 day for adverse and undesirable side effects, 1week & 6 months.
Randomization:
The participants will be randomly assigned to one of the three experimental groups the interventions and control groups using simple randomization with a 1:1 allocation ratio.
Masking/blinding:
Neither the operator nor the patients could be blinded due to the nature of the study but the outcome assessor and statistician will be blinded.
研究类型
研究类型
注册 (估计的)
注册
阶段
阶段
- 不适用
联系人和位置
学习联系方式
学习联系方式
- 姓名:Shaimaa AM Awad, Mcs
- 电话号码:01027557531
- 邮箱:shaimaa.awad@dentistry.cu.edu.eg
研究联系人备份
- 姓名:Aliaa AM Awad
- 电话号码:01062811856
- 邮箱:shaimaa.awad@dentistry.cu.edu.eg
学习地点
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-
-
Cairo、埃及
- Faculty of Dentistry, Cairo University
-
接触:
- Shaimaa Awad, Mcs
- 电话号码:01027557531
- 邮箱:shaimaa.awad@dentistry.cu.edu.eg
-
-
参与标准
资格标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
-
▪ Participants free from any systemic disease aged from 7 years to 12 years
- Anterior permanent teeth with Degree 1(mild) hypomineralization (according to the Wetzel and Reckel scale) (as shown in Appenxix I).
- Enamel opacities, (White, creamy or yellow to brownish colour), without enamel breakdown
- Caries-free teeth.
- Sensitivity to external stimuli e.g., air/water but not brushing.
Exclusion Criteria:
-
▪ Dental caries and filling,
- Loss of the enamel or dentin structure,
- Clinical symptoms of irreversible pulpitis such as spontaneous pain or persisting pain,
- Previous use of bleaching agent.
- Dental anomaly on anterior teeth,
- Periodontal diseases,
- Undergoing orthodontic treatment,
- Cognitive and behavioral conditions.
- Patients with milk protein or hydroxybenzoates allergies.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
手臂数量
武器和干预
参与者组/臂参与者组/臂 |
干预/治疗干预/治疗 |
|---|---|
|
有源比较器:Control group ICON® resin infiltration
Resin infiltration treatment (Icon®) for Hypomineralized anterior permanent teeth in children |
|
|
实验性的:Intervention group 1
Opalustre® Enamel Microabrasion Slurry |
NOTE: For hypo-mineralization greater than 0.1-0.3mm use a fine-grit water-cooled tapered diamond bur, lightly sweep over the stained area for 5-10 seconds prior to applying Opalustre.
|
|
实验性的:Intervention group 2
Antivet® enamel micro-abrasion |
|
研究衡量的是什么?
主要结果指标
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Color enhancement measured by Clinical photographs
大体时间:6 months
|
Clinical photographs will be taken with a digital camera macro lens, and flash. With the patient and digital camera at the same vertical plane and dental clinic illuminated evenly. The photographs will be taken in baseline, during the application time of the test or control. For standardizing the photographic conditions, the camera will be placed at the equidistance from the tooth. To prevent the change of refractive index by moisture, 30 s of drying of the lesion will be done. |
6 months
|
次要结果测量
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Patient satisfaction measured by Visual analogue scale
大体时间:6 months
|
The patient is asked to draw a line perpendicular to the VAS at their perceived pain-intensity level, no discomfort (score 0), mild discomfort (score 1-3), moderate (score 4-6) and very severe (7-9) or worst discomfort (score 10). |
6 months
|
|
Reducing teeth hypersensitivity measured by The Schiff Cold Air Sensitivity Scale (SCASS)
大体时间:6 months
|
It is a behavioral scale because it is based on observed behavior in response to a stimulus beyond a certain threshold. The dentist (or another assessor present) rates the response of the patient to the stimulus as 0 for no response to air stimulus,
|
6 months
|
合作者和调查者
调查人员
调查人员
- 首席研究员:Shaimaa AM Awad, Mcs、Cairo Uviversity
研究记录日期
研究主要日期
学习开始 (估计的)
学习开始
初级完成 (估计的)
初级完成
研究完成 (估计的)
研究完成
研究注册日期
首次提交
首次提交
首先提交符合 QC 标准的
首先提交符合 QC 标准的
首次发布 (实际的)
首次发布
研究记录更新
最后更新发布 (实际的)
最后更新发布
上次提交的符合 QC 标准的更新
上次提交的符合 QC 标准的更新
最后验证
最后验证
更多信息
与本研究相关的术语
其他研究编号
其他研究编号
- 261711198415920202321948291954
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
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研究美国 FDA 监管的设备产品
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