跳至主要内容
临床试验/CTRI/2022/01/039721
CTRI/2022/01/039721已完成4 期

Comparing the incidence of postoperative pain with resin based sealer and calcium silicate based sealer.A prospective clinical trail.

Maheswari1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年2月2日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
postoperative pain

研究概览

简要总结

In this study ,comparing the incidence of postoperative pain by using  calcium silicate based sealer (bio c sealer )and epoxy resin based sealer (AH plus sealer) at 6, 12, 24 and 48 h, and 3, 4, 5, 6 and 7 days. the number of patients taking in this study are 30.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
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

  • •Prolonged positive response to cold test and electric pulp tester Patients diagnosed with asymptomatic and symptomatic irreversible pulpitis caused by deep carious lesio.

排除标准

  • •Patients who refuse to participate this study Medically compromised patients The presence of open apex, presence of calcification, presence of resorption Patients who had allergic sensitivity to local anaesthetic Pregnant patients and patients in lactation period.

结局指标

主要结局

postoperative pain

时间窗: At 6, 12, 24 and 48 hrs, and 3, 4, 5, 6 and 7 days

次要结局

  • analgesic consumption(one week)

研究者

发起方
Maheswari
申办方类型
Other [myself]

研究点 (1)

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