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临床试验/NCT06194773
NCT06194773已完成不适用

Evaluation of the Effect of Totalfil and Neosealer Sealers on the Post-endodontic Pain in Mandibular Molars Diagnosed With Symptomatic Irreversible Pulpitis; a Randomized Control Study.

Gulf Medical University2 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2023年6月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
39
试验地点
2
主要终点
The level of post-endodontic pain

研究概览

简要总结

The goal of this clinical trial is to evaluate the effect of Totalfil and Neosealer sealers on post-endodontic pain compared to AH plus sealer in mandibular molars with symptomatic irreversible pulpitis. The main question: do Totalfil and Neosealer sealers affect postoperative pain intensity after root canal treatment in mandibular molars with symptomatic irreversible pulpitis? Participants will undergo root canal treatment using totalfil, Neosealer, or AH-Plus sealer. Researchers will compare Totalfil, Neosealer, and AH-Plus to assess the intensity of post-endodontic pain.

详细描述

The study will be conducted on 39 mandibular molars; with 13 mandibular mandibular molars in each group (n=13). The patient will be asked to pick an opaque sealed envelope that will contain a number from 1 to 3. The resultant number will determine in which group the participants will be placed. Double blinding will be maintained in this study as the assessor and the patients will not be aware of their group/used root canal sealer.

Group I: Endodontic treatment with obturation using single cone technique with Totalfil sealer.

Group 2: Endodontic treatment with obturation using single cone technique with Neosealer.

Group 3: Endodontic treatment with obturation using single cone technique with AH plus sealer.

Clinical procedure:

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with mandibular molars diagnosed with symptomatic irreversible pulpitis.

排除标准

  • Medically compromised patients.
  • Pregnant patients.
  • Teeth with immature apex formation.

研究组 & 干预措施

Totalfil

Experimental

干预措施: Totalfil (Procedure)

NeoSealer

Experimental

干预措施: NeoSealer (Procedure)

AH-Plus

Active Comparator

干预措施: AH-Plus sealer (Procedure)

结局指标

主要结局

The level of post-endodontic pain

时间窗: 7 days

Evaluation of the pain intensity using the Visual Analogue Scale. The Visual Analogue Scale measures pain intensity. The Visual Analogue Scale consists of a 10 cm with two endpoints representing 0 ('no pain') and 10 ('pain as bad as it could be)

次要结局

未报告次要终点

研究者

发起方
Gulf Medical University
申办方类型
Other
责任方
Sponsor
主要研究者

Rania Zaarour

Senior Researcher at Thumbay Research Institute Coordinator

Gulf Medical University

研究点 (2)

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