Dento-skeletal Effects of Clear Twin Block Treatment at Specific Period in Growing Patients
Dento-skeletal Effects of Clear Twin Block Treatment at Specific Period in Growing Patients: A CBCT Based Controlled Clinical Trial
Aim: To investigate the dento-skeletal effect of clear twin block in patients wearing the appliance at specific period.
Methods: A total of 40 patients (regardless patients sex) with an age ranged from 9 to 12 years with class Ⅱ Div1 mal-occlusion and class 2 skeletal pattern will be included in the study.
All the essential diagnostic records will be taken (for each patient) including:
- Pre-operative and post-operative photographs.
- Pre-operative and post-operative cephalometric radiographs.
- Pre-operative and post-operative digital models.
Another secondary records will be taken include:
- Pre-operative hand and wrist radiograph.
- Pre-operative and post-operative cone beam computed tomography (CBCT) Each patient will wear the appliance for 3 months with 16 hours per day wearing time.
All patient's parents will assign an informed consent describing the treatment protocol.
The following parameters will be assessed:
- Over bite, over jet, inter-canine width and inter-molar width differences on digital models.
- SNA, SNB, ANB, AO-BO and A-B Chang differences on lateral cephalometric radiographs.
- Changes on condylar head and permanent first molar root resorption on CBCT.
研究概览
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习地点
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Baghdad Governorate
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Baghdad、Baghdad Governorate、伊拉克、10001
- 招聘中
- Samer Salim Othman
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接触：
- Samer Salim Othman, Ph.D.
- 电话号码：00964 7805557766
- 邮箱：samerortho@ibnsina.edu.iq
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接触：
- Mohammed Nahidh, Ph.D.
- 电话号码：00964 7702551616
- 邮箱：m_nahidh79@codental.uobaghdad.edu.iq
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-
参与标准
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:
- age ranged from 9 to 12 years
- class Ⅱ Div1 mal-occlusion and class 2 skeletal pattern
Exclusion Criteria:
- Adults (passing the puberty)
- Refuse to participate in the study
- Uncooperative patients
学习计划
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：不适用
- 介入模型：单组作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：Treatment arm
Treatment arm with digital twin block appliance |
Digital twin block used to treat class II skeletal malocclsuion |
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Arch width
大体时间：3 months
|
Maxillary and mandibular inter-molar and premolar widths |
3 months
|
|
CBCT measurements
大体时间：3 months
|
Linear measurements in millimeters |
3 months
|
|
CBCT measurements
大体时间：3 months
|
Angular measurements |
3 months
|
|
CBCT measurements
大体时间：3 months
|
Volumetric measurements in cubic millimeters |
3 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Cephalometric radiographs
大体时间：3 months
|
Cephalometric angular measurements |
3 months
|
|
Cephalometric radiographs
大体时间：3 months
|
Cephalometric linear measurements |
3 months
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- ISU.26.1.25
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
IPD 计划说明
To protect the patinets' privacy
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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