NCT02286648Unknown4 期
Success Rate Evaluation of Miniature Pulpotomy With MTA in Primary Molars
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- successful outcome of treatment as indicated by clinical signs defined with observation and check list
研究概览
简要总结
The purpose of this study is to evaluate the clinical and radiographic success rate of Miniature pulpotomy with Mineral Trioxide Aggregate (MTA) in primary molars.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 4 Years 至 7 Years（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •healthy people(without any systemic disease)
- •no clinical or radiographic evidence of pulp degeneration
- •the possibility of proper restoration of the teeth
排除标准
- •excessive bleeding from the exposure site
- •internal root resorption
- •interradicular and/or periapical bone destruction
- •swelling or sinus tract
研究组 & 干预措施
Mineral Trioxide Aggregate
Experimental
pulpotomy with MTA
干预措施: Mineral Trioxide Aggregate (Drug)
Formocresol
Active Comparator
pulpotomy with FC
干预措施: Formocresol (Drug)
结局指标
主要结局
successful outcome of treatment as indicated by clinical signs defined with observation and check list
时间窗: up to 12 months
success or failure of treatment defined with observation and check list
次要结局
- successful outcome of treatment as indicated by radiographic signs defined with observation and check list(up to 12 months)
研究者
Hossein Nematollahi
principal investigator
Mashhad University of Medical Sciences
研究点 (1)
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