CTRI/2021/12/038942尚未招募不适用
A Clinical and Radiographic Comparative Study Between Zinc Oxide Eugenol Syzygium cumini Mixture, Zinc Oxide Eugenol Propolis Mixture And Zinc Oxide Eugenol As Obturating Materials in Primary Molars: A Randomized Controlled Trial.
Vaviya Saraswati Gangji1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2022年1月1日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 45
- 试验地点
- 1
- 主要终点
- - Clinical evaluation and radiographic evaluation
研究概览
简要总结
This study is a randomized, double blind, parallel group, single centre trial comparing the effectiveness of the zinc oxide eugenol with syzygium cumini mixture, zinc oxide eugenol with propolis mixture and zinc oxide eugenol when used as obturating materials in primary molars will be conducted at Bapuji Dental College and Hospital in Karanataka, India. The standard pulpectomy procedure will be followed by obturation with above mentioned materials. The primary outcome measure will be clinical and radiographic evaluation at 3 months, 6 months, 12 months intervals.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 4.00 Year(s) 至 9.00 Year(s)（—）
- 性别
- All
入选标准
- •One or more of the following criteria will be included for pulpectomy.
- •Caries-affected teeth with intra-oral and/or extra-oral swelling or intra oral draining sinus tract.
- •Teeth with deep caries lesions and associated inter-radicular and/or periapical radiolucency’s.
- •Caries-affected teeth with abnormal mobility due to periapical pathosis, but not associated with normal exfoliation.
- •History of spontaneous pain with tenderness on percussion.
排除标准
- •Primary molars with less than two-thirds of the remaining root length.
- •History of allergic reaction to local anaesthetics.
结局指标
主要结局
- Clinical evaluation and radiographic evaluation
时间窗: Immediate, 3 months, 6 months and 12 months
次要结局
未报告次要终点
研究者
研究点 (1)
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