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临床试验/NCT03942107
NCT03942107已完成不适用

The Effect of Dental Post Application After Root Canal Treatment on Postoperative Pain in Asymptomatic Teeth.

Istanbul Medipol University Hospital2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年4月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
Change from Baseline in Postoperative Pain after post and core application in root canal traeted teeth

研究概览

简要总结

In this study the effect of dental post application on postoperative dental pain in patients with asymptomatic teeth after a single-appointment root canal treatment will be evaluated.

详细描述

The aim of this clinical study is to evaluate the effect of dental post application on postoperative pain intensity level in patients with asymptomatic teeth after a single-appointment root canal treatment. A total of one hundred patients with asymptomatic teeth and with no contradictory medical history who are indicated for non-surgical root canal treatment and application of a dental post at the Endodontic Clinic, Faculty of Dentistry, Istanbul Medipol University, between April and December of 2019 will be included. All of the patients will be recruited from the Istanbul Medipol University Dental Clinics in Istanbul. the patients will be divided in two groups (n=50). Consent will be obtained from all study participants before the treatment. After the root canal treatments are completed in single-visit, in the first groups dental posts will be applied immediately at the same visit and patients will be appointed for pain assessment. In group 2 after the root canal treatment a temporary filling be applied in the access cavity and patients will be appointed for pain assessment. Dental posts will be applied after the pain assessment is completed at the end of 1 week. All treatments will be performed by one endodontist. Postoperative pain intensity will be assessed at 24, 48, and 72 h; 7 days; after the treatment. The teeth will be examined according to postoperative pain intensity levels,

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • patients with asymptomatic teeth which were in need of orthograde non-surgical root canal treatment with post application

排除标准

  • who were younger than 18 years old,
  • who had contradictory medical history for root canal treatment,
  • who used antibiotics 1 month prior and analgesics 1 week prior to the treatment,
  • who could not abide the follow-up time Teeth
  • that were symptomatic
  • with previous root canal treatment
  • with present or suspected vertical root fracture
  • with ≥ 4 mm periodontal pocket depth
  • with apical lesions ≥ 5mm
  • with damaged or resorbed apex
  • that were in need of apical surgery

结局指标

主要结局

Change from Baseline in Postoperative Pain after post and core application in root canal traeted teeth

时间窗: 24, 48, and 72 hours; 7 days

The primary outcome measure of the study is to assess if the application of post and core to restore coronal part of root canal treated teeth may have an additive effect on postoperative pain intensity. Postoperative pain is recorded using vertical Visual Analog Scale (VAS) at 24, 48, and 72-h and 7-day follow-up time by one operator. Patients are asked to mark their pain level on a vertical line with the end points "No pain" and "Worst possible pain". The distance of the marked point to "no pain" end point is measured to calculated pain intensity level. The longer the distance the more the pain intensity level is.

次要结局

未报告次要终点

研究者

发起方
Istanbul Medipol University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tan Firat Eyuboglu

Assistant Professor, Head of Department of Endodontics

Istanbul Medipol University Hospital

研究点 (2)

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