CTRI/2025/08/093058尚未招募2/3 期
Clinical evaluation of a nano-ceramic composite resin and a resin-modified glass ionomer restorative in non-carious cervical lesions: a split-mouth randomised controlled trial
Sravya Tadiparthi1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2025年8月25日最近更新:
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 46
- 试验地点
- 1
- 主要终点
- To evaluate the clinical performance of two different posterior restorative materials using FDI criteria
研究概览
简要总结
Forty six patients with age group between 30 to 60 years who are having atleast two posterior teeth in two different quadrant with moderate non-carious cervical lesions will be recruited in the study. Selected teeth will be divided into two groups. Restoration survival and clinical performance will be evaluated at baseline, 3 months, 6 months, 9 months, 12 months and 18 month visits
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
- 30.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients with no serious systemic diseases.
- •Patients with at least four non-carious cervical lesions.
- •Patients with cervical margins in dentin.
- •Patient with vital pulp with the absence of symptoms of pulpitis.
排除标准
- •Patients with a history of bruxism or parafunctional habits.
- •Teeth with chronic periodontal involvement and gingival inflammation.
- •Teeth that are grossly decayed.
- •Patients with very poor oral hygiene, Patients suffering from psychological or neurological conditions.
结局指标
主要结局
To evaluate the clinical performance of two different posterior restorative materials using FDI criteria
时间窗: baseline(0 months)
次要结局
- To evaluate the clinical survival & performance of two different restorative materials(3 months, 6 months, 9 months, 12 months & 18 months)
研究者
Sravya Tadiparthi
GITAM dental college and hospital
研究点 (1)
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