IRCT2016012126137N1已完成未知
Comparison of post operative pain in necrotic pulp using two different instrumention techniques : A Randomized Clinical Trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 no limit（—）
- 性别
- All
入选标准
- •inclusion criteria : age over 18-year-old ; no systemic disease necrotic pulp without pain before treatment ; normal or periapical lesion less than 2.5mm ; sensivity on percussion ; no sensivity on palpation ; restorable, no sinus tract or apical abscess or facial cellulite
- •exclusion criteria : age lower than 18-year-old ; systemic disease ; pregnancy,milking mother,allergy to lidocaine ,normal pulp, pulpit,normal periapical or periapcal lesion greater than 2.5mm ; failure in anesthesia ; bleeding after coronal access ; intake of analgesics 48 -72 hours before treatment ; intake of cortone one week before treatment ; sensivity on palpation
排除标准
- 未提供
研究者
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