Comparison of postoperative sensitivity of Bulk Fill composite using a two step technique with incrementally layered Nanocomposite in class 1 cavities and selective etch method: A Randomized Controlled Single Blind Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Postoperative sensitivity scores
研究概览
简要总结
Restorative dentistry deals with the treatment of tooth defects and restores the function without compromising the biology. Poor adaptation can lead to postoperative sensitivity and failure of restoration. There are problems associated with using resin composite in posterior restorations, most important of which is shrinkage that occurs on setting, and causes postoperative sensitivity. Incremental filling technique reduces polymerization shrinkage by reducing the C-factor, but it has some drawbacks, like incorporation of voids between layers or contamination. These drawbacks have led some manufacturers to introduce composite resins for bulk filling techniques. The bulk fill composite resins have low volumetric shrinkage, but studies have reported that placement of thick increments may increase the stress at the adhesive interface, which may increase postoperative sensitivity. Studies have however reported that the filling technique has no influence on polymerization shrinkage at adhesive interface. Despite the presence of various placement techniques and developments in the technology of resin composites clinical failures of composite restorations are still present. To the best of our knowledge, incidence of postoperative sensitivity using 3M Filtek Z350XT Nanofill composite and 3M Filtek Bulk fill composite has not been evaluated yet. Hence this study is designed to compare and evaluate the postoperative sensitivity of Nanocomposite [3M Z350XT] using incremental layering technique and Bulk fill composite [3M Bulk fill] using a 2 step technique in class 1 cavities.
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 65.00 Year(s)(—)
- 性别
- All
入选标准
- •Cooperative, healthy subjects who are willing to participate in the study and sign the consent form.
- •Molars and premolars requiring Class 1 composite resin restorations for the treatment of primary carious lesions.
- •Carious lesions involving enamel and dentin [ICDAS score 3, 4 &5] clinically and radiographically [ICDAS score RA2, RA3 & RB4].
- •Asymptomatic patient or patient having symptomatic reversible pulpitis.
- •The selected teeth should have occlusal contacts with natural or crowned antagonist teeth.
- •Vital teeth giving a positive response to cold test.
排除标准
- •Subjects unwilling to sign the consent form.
- •Teeth with deep carious lesions approaching the pulp.
- •Patients having old restorations.
- •Teeth with spontaneous, severe or continuous pain.
- •Patients with any irreversible pulpal, periodontal and periapical pathology.
- •Patients with painful temporomandibular joint problems.
- •Patients taking analgesics and anti-inflammatory drugs during past 3 days.
- •Patients having bruxism.
结局指标
主要结局
Postoperative sensitivity scores
时间窗: Postoperative sensitivity scores at 24 hours 48 hours & 7 days
次要结局
- Effect of depth of cavity on postoperative sensitivity(After 24 hours 48 hours & 7 days)
