跳至主要内容
临床试验/NCT06231290
NCT06231290招募中不适用

The Influence of Magnification and Clinical Experience on the Outcome of Pulpotomy in Mature Adult Teeth: A Randomized Clinical Trial

Al-Azhar University2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2024年3月20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
68
试验地点
2
主要终点
Clinical and radiographic outcome

研究概览

简要总结

The goal of this interventional randomized clinical trial is to test the effect of magnification and clinical experience of the operator on the success rate of full pulpotomy in mature adult molar teeth.

The main questions it aims to answer are:

  • Does the use of magnification raise the success rate of full pulpotomy of mature adult molars?
  • Does the clinical experience of the operator dentist raise the success rate of full pulpotomy of mature adult molars?

Participants will be asked to do the following:

  • Receive the pulpotomy treatment of their target molar tooth.
  • Record the pain score in the pain assessment chart.
  • Attend the follow-up visits. They'll receive a full pulpotomy treatment of their target molar tooth. Researchers will evaluate the usage of magnification in performing the pulpotomy procedure of adult molar teeth by postgraduate or undergraduate operators in comparison to performing the same pulpotomy procedure without magnification to see if it raises the overall success rate of pulpotomy.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy patients diagnosed with acute irreversible pulpitis related to maxillary or mandibular permanent molar teeth without apical periodontitis.

排除标准

  • Non-vital teeth.
  • Immature teeth.
  • Presence of swelling or sinus tract.
  • Teeth with mobility grade II or III.
  • Immunocompromised patients.
  • Non-restorable teeth.
  • Teeth with apical periodontitis seen in periapical radiograph.
  • Periodontally affected teeth.
  • Teeth with reversible pulpitis
  • Extensive non-stoppable bleeding more than 6 minutes
  • Teeth with partial necrosis

结局指标

主要结局

Clinical and radiographic outcome

时间窗: Immediately, 1, 3, 6 and 12 months.

The clinical outcome will be measured by the presence or absence of signs and symptoms. The radiographic outcome will be measured by using the PAI index which is a scale from 1 (best) to 5 (worst).

次要结局

  • Postoperative pain(Immediately, 24, 48, 72 hours and 7 days)

研究者

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

Mohamed Ahmed Mohamed Yahia

Postgraduate student

Al-Azhar University

研究点 (2)

Loading locations...

相似试验