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临床试验/NCT05726357
NCT05726357招募中不适用

Pulpotomy vs Root Canal Treatment for Teeth With Symptomatic Irreversible Pulpitis: A Randomised Control Trial

British University In Egypt2 个研究点 分布在 1 个国家目标入组 380 人开始时间: 2023年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
380
试验地点
2
主要终点
pain score

研究概览

简要总结

high-quality evidence is needed to add to current knowledge and also assess the long-term outcomes for full/complete pulpotomy after carious pulpal exposure in patients with signs and symptoms indicative of irreversible pulpitis

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • a mature permanent tooth
  • symptoms indicative of IRP
  • responsive to cold and EPT sensibility testing
  • restorable and can be adequately isolated during treatment
  • One tooth (molar or premolar) per patient.

排除标准

  • active periodontal disease
  • complex medical histories
  • unable to consent
  • pregnant or breast-feeding
  • excessive bleeding that cannot be controlled

结局指标

主要结局

pain score

时间窗: day 3 post treatment

score by a numeric rating scale from 1(minimum pain) to 100 (maximum pain)

次要结局

  • pain score(6 months post treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

shehabeldin saber

Professor

British University In Egypt

研究点 (2)

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