跳至主要内容
临床试验/CTRI/2023/08/056102
CTRI/2023/08/056102尚未招募2/3 期

Comparative evaluation of postoperative pain in multi-visit root canal treatment using three different rotary files system- A randomized clinical trial

Saveetha Dental College and Hospital1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2023年1月9日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
75
试验地点
1
主要终点
To assess the post instrumentation pain by visual Analog Scale at 6hrs, 12hrs, 24hrs, 48hrs & 72 hours after instrumentation

研究概览

简要总结

Post-operative pain is defined as pain of any degree that occurs after initiation of root canal treatment(RCT) (Sathorn et al. 2007). Although microorganisms are regarded as the primary cause of postoperative pain, inevitable extrusion of the irrigant solution, or debris that contain necrotic tissue,microorganisms, pulpal fragments and dentine particles from the root canal space into theperiradicular tissues may also lead to post operative pain (Seltzer et al. 1985). There has been a paradigm shift from the use of stainless steel hand files to rotary NiTi files and morerecently to reciprocating NiTi instruments. The instruments along with the preparation techniqueshave been considered as the principal contributing factor resulting in debris extrusion (Al-Omari et al.1985, Fairbourn et al. 1987, Kustarci et al. 2008, Yeter et al. 2013).

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patient with irreversible pulpitis.
  • 18 years of age to 60
  • Maxillary and mandibular 1st and 2nd molar
  • Root canal curvature less than 20 degrees in Schneider’s technique
  • PAI score less than 2.

排除标准

  • Patient with periapical cyst and abscess.
  • Pain scale value of more than 6
  • Presence of root caries or root fracture, sinus opening, swelling, Periodontally compromised teeth
  • Grade 2 or grade 3 mobility
  • Patients with systemic diseases and pregnant patients.
  • Patient has taken medication in the last 24 hrs.
  • Informed consent and not willing to participate in the study protocol.

结局指标

主要结局

To assess the post instrumentation pain by visual Analog Scale at 6hrs, 12hrs, 24hrs, 48hrs & 72 hours after instrumentation

时间窗: visual Analog Scale at 6hrs, 12hrs, 24hrs, 48hrs & 72 hours

次要结局

未报告次要终点

研究者

发起方
Saveetha Dental College and Hospital
申办方类型
Research institution and hospital

研究点 (1)

Loading locations...

相似试验