Evaluation of adhesion strategies in restoration of Non Carious Cervical Lesions extending to root surface-a randomized controlled trial
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Comparison of Clinical performance between two universal adhesive agents using USPHS criteria
研究概览
简要总结
The aim of the study is to evaluate the clinical performances of two adhesive agents. The patients will be randomized to the following groups by simple randomization.GROUP 1: Total Etch (Etch and rinse - 5th Generation), GROUP 2: Universal Adhesive in Self Etch(8th Generation), GROUP 3: Universal Adhesive in Selective Enamel Etch(8th Generation), all the Restorative procedure will be carried out by a single operator. Adhesive protocol will be followed as per the randomization schedule. Restoration will be done using Nano Hybrid Composite. The patient and outcome assessor will be blinded to the study, making it a double-blinded randomized controlled trial. The patient will be evaluated by two independent calibrated examiners at time intervals of 1, 3, 6, 12 and 18 months using USPHS criteria.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 85.00 Year(s)（—）
- 性别
- All
入选标准
- •Teeth with Non Carious Cervical Lesions extending to the root Depth of non carious cervical lesion should be more than 1 mm.
排除标准
- •History of existing tooth hypersensitivity Bruxism Cervical Caries Non-vital teeth Known inability to return for recall Appointments Fractured or visible cracked teeth Medically compromised patients Allergy to components of resin-based materials Existing periodontal disease Third molar Sub gingival lesion.
结局指标
主要结局
Comparison of Clinical performance between two universal adhesive agents using USPHS criteria
时间窗: 1,3,6,12 and 18 months
次要结局
- Pulpal and Periodontal Health at the end of follow up periods.(1,3,6,12 and 18 months)