CTRI/2021/08/035494招募中不适用
Comparative Evaluation of Clinical Efficacy of Different Restorative Materials in Class V Lesions: An In Vivo Study
Dr Tanu1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2021年8月15日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 300
- 试验地点
- 1
- 主要终点
- To Evaluate and Compare Clinical Efficacy Of Newer Alkasite Material and Composite using USPHS Criteria
研究概览
简要总结
The Purpose of this study is Comparative evaluation of clinical efficacy of cention N and composite in non carious class V Cervical lesions . The sample size of this trial is 300 which is divided into two groups of 150 each . The followup will be done at 3, 6, 9 months and 1 year using USPHS Criteria .
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 75.00 Year(s)（—）
- 性别
- All
入选标准
- •Inclusion criteria Subjects with fair oral hygiene Saucer shaped or V shaped cervical lesions Maxillary and mandibular canine and posterior teeth Vital teeth Teeth with occlusion and inter proximal contact Subjects with age between 18–75 years.
排除标准
- •Carious cervical lesions.
结局指标
主要结局
To Evaluate and Compare Clinical Efficacy Of Newer Alkasite Material and Composite using USPHS Criteria
时间窗: Assessed at 3,6,9 months and 1 year | Â
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时间窗: Assessed at 3,6,9 months and 1 year | Â
次要结局
未报告次要终点
研究者
研究点 (1)
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