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临床试验/CTRI/2020/03/023766
CTRI/2020/03/023766尚未招募不适用

Comparitive Evaluation Of Post Operative Pain And Success Rate Of MTA Pulpotomy And Biodentine Pulpotomy And Root Canal Treatment In Cariously Exposed Permanent Molars And Premolars: An In Vivo Study

Mandeep S Grewal1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2020年5月3日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
150
试验地点
1
主要终点
No post operative pain and successful treatment outcome

研究概览

简要总结

cariously exposed mature premolar and molar teeth with irreversible pulpitis were allocated in three groups. in the first group pulpotomy was done using MTA, in the second group pulpotomy was done using biodentine and in the third group root canal treatment was performed and the patients were recalled at subsequent follow up visits for evaluating the post operative pain and success rate of pulpotomy as compared to root canal therapy. groups in which pulpotomy was performed, if reported with pain then root canal therapy was initiated for those patients.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 69.00 Year(s)(—)
性别
All

入选标准

  • •Periodontally healthy maxillary and mandibuar permanent molars and premolars with the carious exposure of pulp will be included.
  • •Age criteria- patients ranging from 18 to 69 years of age will be incuded in the study.
  • •Positive response to vitality tests and a history of pain and presenting symptoms characteristic of symptomatic irreversible pulpitis according to American Association of Endodontics diagnosis terminology, but in the absence of sinus tract or swelling will be included.

排除标准

  • ••Immunocompromised patients •Patients having negative response to vitality tests •Positive history of intake of antibiotics use in the past one month or requiring antibiotic prophylaxis.
  • ••Tooth previously accessed.
  • ••Association of periapical lesion visible on the radiograph.
  • ••Cases in which the bleeding could not be controlled upto fifteen minutes.

结局指标

主要结局

No post operative pain and successful treatment outcome

时间窗: 1 year

次要结局

  • Pain or swelling at follow up visits(1 year, 6 months)

研究者

发起方
Mandeep S Grewal
申办方类型
Other [self]

研究点 (1)

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