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
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
- 是
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
Mohamed Ahmed Mohamed Yahia
Postgraduate student
Al-Azhar University
研究点 (2)
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