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临床试验/NCT06437197
NCT06437197已完成不适用

Clinical and Radiographic Evaluation of Platelets Rich Fibrin in Adult Pulpotomy: Randomized Clinical Trial

Al-Azhar University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年3月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
Radiographic changes in periapical area using periapical radiographs.

研究概览

简要总结

The goal of this interventional randomized clinical trial is to evaluate the use of platelet rich fibrin in full pulpotomy in mature adult teeth.

The main questions it aims to answer are:

  1. Does the use of platelet rich fibrin in complete pulpotomy in mature permanent teeth will raise the success rate of full pulpotomy of adult teeth?
  2. Does the use of cone beam computed tomography scans will be more effective in early detection of apical periodontitis than periapical radiographs?

Participants will be asked to do the following:

  • Receive the pulpotomy treatment of their target 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 tooth. Researchers will evaluate the usage of platelet rich fibrin in performing the pulpotomy procedure of adult teeth and if cone beam computed tomography scans will be more effective in early detection of apical periodontitis than periapical radiographs.

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 (Participant)

入排标准

年龄范围
25 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patient age: 25-35 years
  • Mature permanent premolar teeth with two separate roots.
  • Clinical diagnosis of irreversible pulpitis.
  • Patients without existing medical condition.
  • Exclusion criteria:
  • Immature teeth.
  • Non-restorable teeth.
  • Non-vital Teeth.
  • Uncontrolled pulpal bleeding.
  • Periodontally affected teeth.

排除标准

  • 未提供

结局指标

主要结局

Radiographic changes in periapical area using periapical radiographs.

时间窗: 6 and 12 months.

The radiographic changes was evaluated using periapical radiographs. the outcome was measured using the periapical index scoring 1,2,3,4 or 5 with 1 indicating normal and 5 indicates severe periodontitis with exacerbating features.

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

Ahmed Ibrahim Ahmed Qandeel

Demonstrator of Endodontics, Faculty of Dental Medicine

Al-Azhar University

研究点 (2)

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