Effectiveness of Two Skeletally Anchored Force Mechanics for Skeletal Class II Correction in Growing Patients
2022年7月25日 更新者:Yasmine Mohamed Sayed Mahmoud、Alexandria University
Effectiveness of Two Skeletally Anchored Force Mechanics for Correction of Skeletal Class II Malocclusion in Growing Patients (A Randomized Controlled Clinical Trial)
Patients with skeletal Class II malocclusion due to mandibular retrognathism will be recruited and randomly allocated to three equal groups.
first group will be treated by pushing orthopedic force mechanics, second group will be treated by pulling orthopedic force mechanics, and third group will be observed for 9 months to detect the natural growth changes.
Skeletal changes will be evaluated and the treatment changes will be compared with the natural growth changes.
The study hypothesis is that use of direct bimaxillary miniplate anchorage in conjunction with fixed functional appliance (pushing orthopedic force) or closed coil spring (pulling orthopedic force) will induce statistically significant skeletal mandibular growth in comparison to natural mandibular growth changes.
研究概览
地位
主动,不招人
条件
详细说明
A randomized controlled clinical trial will be conducted to address the aim of the study.
Thirty-nine growing patients with skeletal Class II malocclusion due to mandibular retrognathism will be recruited.
The sample will be randomly allocated to three equal groups, each including thirteen subjects.
Group A will be treated by pushing orthopedic force mechanics using fixed functional appliance (Sabbagh Advanced Repositioning Appliance) anchored to four miniplates (two miniplates inserted in the mandibular symphysis and two infrazygomatic miniplates), and Group B, will be treated by pulling orthopedic force mechanics using Class II springs (CS Class II correction device) anchored to four miniplates (two inserted in the mandibular posterior buccal segment and two inserted in the maxillary anterior segment).
In both groups, the appliances will be removed after reaching an edge-to-edge incisor relationship or after 9 months, whichever happens first.
A similar third group (Group C) will be observed for 9 months to detect the natural growth changes.
Skeletal changes will be evaluated using pretreatment and posttreatment cone beam computed tomography scans (CBCT).
The treatment changes will be compared with the natural growth changes observed in group C. Other variables will be also examined including, the dentoalveolar effects, the soft tissue profile, and the patient's acceptance to this treatment modality.
研究类型
介入性
注册 (预期的)
39
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
-
Alexandria、埃及、21526
- Faculty of Dentistry
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
11年 至 13年 (孩子)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Chronological age ranges from 11 years to 13 years.
- Skeletal Class II malocclusion with a deficient mandible (SNB ≤ 76°).
- Horizontal growth pattern (MP/SN ≤ 39°).
- Angle Class II division 1 malocclusion with at least 5 mm overjet.
- Mandibular arch crowding less than 5 mm.
- The patients have to be in the prepubertal growth stage (cervical maturational stage 3 or 4) when applying orthopedic force.
- Patients with good oral hygiene, and a healthy periodontal condition.
Exclusion Criteria:
- Patients who underwent previous orthodontic treatment.
- Patients with previous craniofacial surgeries, chronic diseases, syndromes, or growth problems that may affect bone.
- Any signs or symptoms of para-functional habits or previous history of temporomandibular disorders.
- Extracted or missing upper permanent teeth (except for third molars).
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
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:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Miniplates in mandibular symphysis & infrazygomatic
|
Fixed functional appliance (pushing orthopedic force) in conjunction with direct skeletal anchorage
|
|
有源比较器:Miniplates in external oblique ridge & anterior maxillary region
|
Coil spring (pulling orthopedic force) in conjunction with direct skeletal anchorage
|
|
无干预:Growing skeletal Class II subjects
|
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 |
|---|---|---|
|
change in the effective mandibular length (Co-Gn)
大体时间:at baseline and after treatment completion about 9 months
|
Correction of the skeletal Class II relation.
This outcome will be detected by measuring the mean change in the effective mandibular length (Co-Gn) and position on CBCT images from baseline data (T1) and after appliance removal (T2) and will be compared with the growth changes observed in the control group
|
at baseline and after treatment completion about 9 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
change in maxillary length (Co-A)
大体时间:at baseline and after treatment completion about 9 months
|
The effective maxillary length (Co-A) and position changes will be measured after and chin will be measured.
|
at baseline and after treatment completion about 9 months
|
|
Changes in the soft tissue angle of convexity
大体时间:at baseline and after treatment completion about 9 months
|
the position of the upper and lower lips, and chin will be measured.
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at baseline and after treatment completion about 9 months
|
|
patient acceptance of treatment
大体时间:After treatment completion about 9 months
|
The patient's acceptance to the treatment will be evaluated using a visual analog scale questionnaire after removal of the appliances.
|
After treatment completion about 9 months
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2021年3月8日
初级完成 (预期的)
2022年12月1日
研究完成 (预期的)
2022年12月1日
研究注册日期
首次提交
2021年4月24日
首先提交符合 QC 标准的
2021年5月10日
首次发布 (实际的)
2021年5月12日
研究记录更新
最后更新发布 (实际的)
2022年7月27日
上次提交的符合 QC 标准的更新
2022年7月25日
最后验证
2022年7月1日
更多信息
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