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临床试验/CTRI/2021/11/038198
CTRI/2021/11/038198尚未招募2 期

Evaluation of post-operative sensitivity in non carious cervical lesions using two Universal adhesives in different adhesive strategies - A Double-blinded Randomized controlled clinical trial.

Saveetha Dental College and Hospitals1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年1月12日最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Reduced VAS score for assessment of postoperative sensitivity at 24 hrs, 1week, 2weeks, 4 weeks.

研究概览

简要总结

Post-operative sensitivityis one of the main complications occurring after placing compositerestorations. Although there may be numerous reasons for its occurrence,adhesives play an important role. The introduction of Universal adhesives,  has significantly eased the process ofadhesion for the clinician since the same adhesive can be used in variousstrategies of adhesion (total etch, self etch, selective etch). But the use ofdifferent adhesive strategies may cause post-operative sensitivity. This studywill help understand the effect of adhesive strategy used on the post-operativesensitivity

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
30.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • •patients 30-50 years of age atleast 2 NCCLs in each quadrant depth of the lesion 1-3mm, presence of antagonist teeth.

排除标准

  • •poor gingival and periodontal health; uncontrolled rampant caries; bruxism; patients with systemic diseases.

结局指标

主要结局

Reduced VAS score for assessment of postoperative sensitivity at 24 hrs, 1week, 2weeks, 4 weeks.

时间窗: 24 hrs, 1week, 2weeks, 4 weeks.

次要结局

未报告次要终点

研究者

申办方类型
Research institution and hospital

研究点 (1)

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