跳至主要内容
临床试验/CTRI/2026/02/104351
CTRI/2026/02/104351尚未招募4 期

A Comparative evaluation of post operative pain with ultrasonically activated Irrigants- Triton vs 3 percent NAOCL in teeth with symptomatic irreversible pulpitis-A Randomized Clinical Study

Dr Chandni Shah1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2026年3月3日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
32
试验地点
1

研究概览

简要总结

This study helps us to evaluate and compare the post-operative pain with  Ultrasonically acticated 3% NAOCL and Triton  as root canal irrigants  in teeth with pulpal diagnosis of symptomatic irreversible pulpitis at 6 hrs,12 hrs,24 hrs and 48 hrs.

研究设计

研究类型
Interventional
分配方式
Randomized
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

  • Healthy patients (Category: American Society of Anaesthesiologists class 1) (ASA House of Delegates 2014) aged between 18 to 60 years of age will be included.
  • Patients with preoperative pain scores ranging from moderate to severe (4 to 10) on a visual analog scale (VAS scale).
  • Patients responding positive to pulpal sensitivity by Electronic pulp Test or Thermal stimuli will be included.
  • 4.Maxillary or Mandibular teeth diagnosed with Symptomatic irreversible pulpitis with or without periapical pathology or radiographic rarefaction.
  • (PAI score less than 3) 5.Only those patients ready to sign the consent form will be included in the study.

排除标准

  • 1.Teeth with open apex, root resorption and calcified pulp chamber and canals will be excluded from the study.
  • 2.Teeth with curvature more than 20 degree will be excluded from the study 3.Patients taking analgesics 12 hours before the intervention.
  • 4.Teeth which had received previous endodontic treatment will be excluded from the study.
  • 5.Cases showing periodontal pockets deeper than 4mm will be excluded from the study.
  • 6.Teeth with pre-op swelling, draining sinus and Flare ups during root canal treatment will be excluded from the study.
  • 7.Any other iatrogenically affected root canal treatments will be excluded from the study.
  • 8.Medically compromised patients will be excluded from the study.

研究者

发起方
Dr Chandni Shah
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Chandni shah

K M Shah Dental College and Hospital

研究点 (1)

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