跳至主要内容
临床试验/CTRI/2024/06/068984
CTRI/2024/06/068984尚未招募2 期

Preserving Vitality- Comparative evaluation of three bioactive materials used in pulpotomy of mature permanent teeth

Mohil Kale1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2024年7月1日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
45
试验地点
1
主要终点
Reduction of pain measured by VAS score

研究概览

简要总结

Until recently, the pulp of mature tooth exposed by caries was considered as a "doomed organ", with pulp extirpitation and root canal treatment being the standard treatment protocol

In cases involving pulp exposure to the level of coronal pulp, pulpotomy has emerged as a treatment protocol as it aids in preserving the vitality of the tooth

Preservation of pulpal vitality of of paramount importance as vital functioning of pulp is capable of initiating several important functions such as formation of dentin, providing nutritive support, enabling a defensive function and possessing a unique regenerative capacity

Pulpotomy is a procedure which involves removal of inflammed coronal pulpal tissue and replacing it with a suitable material, leaving vital radicular pulp within the canals

The advent of newer bioactive materials like Mineral Trioxide Aggregate (MTA), Biodentine and bioceramics have significantly increased the prognosis of vital pulp therapy

The aim of this study is to evaluate and compare performance of three different bioactive materials as pulpotomy agents in mature permanent molars

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

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

入选标准

  • Mandibular molars with caries extending to pulp and having symptoms of irreversible pulpitis with positive response to vitality tests (Cold test+EPT).

排除标准

  • Teeth that will not respond to vitality tests (Cold+EPT) Teeth with periapical involvement Individuals having Systemic diseases or on antibiotics Teeth having excessive bleeding after cavity preparation (Haemostasis not achieved within 5 minutes of coronal pulp removal).

结局指标

主要结局

Reduction of pain measured by VAS score

时间窗: Baseline

次要结局

  • Elimination of pain measured by VAS score(After 7 days, 1 month, 3 months, 6 months, 1 year)
  • No pathosis evident on radiograph(After 7 days, 1 month, 3 months, 6 months, 1 year)

研究者

发起方
Mohil Kale
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Mohil Kale

College Of Dental Sciences And Research Center

研究点 (1)

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