NCT01962077已完成不适用
Comparison of MedCem MTA and Formocresol Used in Pulpotomies in Primary Teeth
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Success of MedCem MTA pulpotomy in primary molar
研究概览
简要总结
assess the effect of MedCem MTA as a pulp medicament following pulpotomy in human primary molars with carious pulp exposure in comparison to Formocresol.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 2 Years 至 10 Years（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •healthy children
- •with Asymptomatic primary molars with a deep carious lesion;
- •Exposure of a vital pulp by caries;
- •No clinical or radiographic evidence of pulp degeneration, such as excessive bleeding from the root canal, internal root resorption, inter-radicular and/or periapical bone destruction,swelling, or sinus tract;
- •Ability to perform a leakage free restoration of the teeth using stainless steel crown, or amalgam/resin based restoration.
排除标准
- 未提供
研究组 & 干预措施
MedCem MTA pulpotomies
Experimental
干预措施: MedCem MTA pulpotomies in primary teeth. (Procedure)
结局指标
主要结局
Success of MedCem MTA pulpotomy in primary molar
时间窗: Up to 36 months
No pain, no swelling or sinus tract, no internal root resorption progressing into the bone, no furcation and/or periapical bond destruction.
次要结局
未报告次要终点
研究者
研究点 (1)
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