跳至主要内容
临床试验/NCT05729893
NCT05729893招募中不适用

Evaluation of Post Operative Pain After Using Two Different Types of Sealers (a Randomized Clinical Trial )

British University In Egypt1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 12 hours

研究概览

简要总结

conventional endodontic treatment is done using two different types of sealers in the obturation to evaluate the post operative pain between the two sealers

详细描述

STUDY WILL BE PERFORMED ON PATIENTS DIAGNOSED WITH SYMPTOMATIC IRREVERSABE PULPITIS.

TREATMENT PROTOCOL FOR ALL PATIENTS IS CONVENTIONAL ROOT CANAL TREATMENT

ACCESS CAVITY AND CLEANING AND SHAPING PROCEDURES WILL BE EXECUTED FOR ALL PATIENTS WITH THE SAME PROTOCOL

SELECTED PATIENTS WILL THEN BE DIVIDED INTO TWO GROUPS,

GROUP1: ALL CANALS WILL BE OBTURATED USING RESIN STANDARD SEALERS.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Patients were randomly divided into two groups according to material used for obturation . each patients name will be replaced with a case number within the group to protect the privacy of medical information and data of the patients care provider and the investigator will not know the name of the patient and the assessor doesn't know the group he is assessing

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •• Patients age ranges from 18-50 years old.
  • •Patients with teeth diagnosed with symptomatic irreversible pulpitis.
  • •Normal periapical condition confirmed by normal periapical radiograph or that with minimal widening of the PDL space
  • •The teeth are restorable
  • •Teeth are periodontally free.

排除标准

  • •• Teeth with immature roots
  • •Non restorable teeth
  • •Medically compromised patients with systemic complication that would alter the treatment.
  • •Necrotic teeth
  • •Teeth with apical periodontitis or periapical lesions
  • •Teeth that need multiple visits treatment

研究组 & 干预措施

resin group

Active Comparator

obturated with resin sealer

干预措施: root canal sealers (Other)

bio ceramic group

Active Comparator

obturated with bioceramic sealer

干预措施: root canal sealers (Other)

结局指标

主要结局

Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 12 hours

时间窗: 12 hours

Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.

Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 24 hours

时间窗: 24 hours

Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.

Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 48 hours

时间窗: 48 hours

Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.

Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 72 hours

时间窗: 72 hours

Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line.

次要结局

未报告次要终点

研究者

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

Sara Alsayed Endo

principal investigator

British University In Egypt

研究点 (1)

Loading locations...

相似试验