Assessment of Two Different Modalities of Maxillary Canine Retraction Assisted With Micro-osteoperforations Versus Injectable Platelet Rich Fibrin: A Comparative Clinical Study
试验速览
- 阶段
- 2 期
- 状态
- Enrolling By Invitation
- 入组人数
- 18
- 试验地点
- 1
- 主要终点
- Direct clinical assessment of the amount of maxillary canine retraction i.e. amount of extraction space closure before and after four months observation period and on every 28 days observation period according to standardized method
研究概览
简要总结
The present clinical comparative study will be undertaken for assessment of two different modalities of maxillary canine retraction assisted with microosteoperforations versus injectable platelet rich fibrin.
详细描述
Group I: will include 9 patients who willreceive MOPs with maxillary canine retraction that will be performed on intervention sides according to a standardized protocol.
▪ Group II: will include 9 patients receive i-PRF that will be performed on intervention sides according to a standardized protocol.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Factorial
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 15 Years 至 22 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •An age ranges from 15-22 years.
- •Severe crowding or protrusion requiring 1st premolars extractions followed by symmetrical canine retraction.
- •All permanent teeth present, 3rd molars are excluded.
- •Good oral and general health.
- •No systemic disease/medication that could interfere with OTM.
- •No previous orthodontic treatment.
排除标准
- •Patient diagnosed to have an indication for non-extraction approach.
- •Poor oral hygiene or periodontally compromised patient.
- •Patient with craniofacial anomalies or previous history of trauma, bruxism or parafunctions.
- •Previous orthodontic treatment.
研究组 & 干预措施
Group MOPs
Group MOPs : will include 9 patients who willreceive MOPs with maxillary canine retraction that will be performed on intervention sides according to a standardized protocol.
干预措施: injectable platelet rich fibrin versus microosteoperforation (Combination Product)
Group IMOPS
other side in group which is control group
Group i-PRF
group i-PRF: will include 9 patients receive i-PRF that will be performed on intervention sides according to a standardized protocol
干预措施: injectable platelet rich fibrin versus microosteoperforation (Combination Product)
group i-PRF2
other side in group which is control group
结局指标
主要结局
Direct clinical assessment of the amount of maxillary canine retraction i.e. amount of extraction space closure before and after four months observation period and on every 28 days observation period according to standardized method
时间窗: 4months
Direct clinical assessment of the amount of maxillary canine retraction i.e. amount of extraction space closure before and after four months observation and every 28 days period and on every 28 days observation period according to standardized method. 2. Study cast assessment: • The amount of maxillary canine retraction on both sides will be measured immediately before starting canine retraction and at each observation interval by using a software for the scanned models according to standardized method
次要结局
未报告次要终点
研究者
farouk ahmed hussein
Principal Investigator
Al-Azhar University