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临床试验/CTRI/2023/05/053313
CTRI/2023/05/053313已完成不适用

Evaluation and comparison of bio-ceramic and resin based sealer along with two types of irrigating needles on post operative pain and quality of life in mandibular molar teeth with symptomatic irreversible pulpitis – A randomized clinical trial

YASMEEN MOHAMMED AZEEM1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年6月15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
60
试验地点
1
主要终点
post operative pain evaluation using visual analogue scale.

研究概览

简要总结

Bio-ceramicmaterials have shown to improve the treatment outcome by promoting thedifferentiation of odontoblasts and by releasing biologically activesubstances. Postoperative pain is multifactorial, so it is very difficult toconsider every factor potentially involved in its aggravation or diminution.So, this trial is being conducted to evaluate and compare the postoperativepain by using different irrigation needles (conventional and side vented) forirrigation and bio-ceramic and resin based sealers for obturation.

研究设计

研究类型
Interventional
分配方式
Random Number Table
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • •a.Patients with symptomatic irreversible pulpitis (mandibular molar).
  • •b.Healthy patients of age group between 18-55 yrs.
  • •c.Patients with preoperative pain scores which will vary from moderate to severe pain on a visual analog scale (VAS).
  • •d.Patients who will have the ability to understand and to use the pain scale.

排除标准

  • ••Patients with any uncontrolled systemic diseases.
  • ••Retreatments of root canals.
  • ••Teeth with immatureopen apex.
  • ••Patients who initiated root canal treatment in other clinics.
  • ••Patients who has taken analgesic or anti-inflammatory drugs within the last 12 hours.
  • ••Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine.
  • ••Pregnant and lactating mothers.
  • ••Patients who are unable or unwilling to complete the pain questionnaires.
  • ••Patients who are unwilling to sign consent for endodontic treatment.

结局指标

主要结局

post operative pain evaluation using visual analogue scale.

时间窗: 6, 24, 48, 72 hours and on 7th day after the endodontic treatment

次要结局

  • quality of life assessment(7th day after root canal treatment)

研究者

发起方
YASMEEN MOHAMMED AZEEM
申办方类型
Other [self]

研究点 (1)

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