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临床试验/CTRI/2021/01/030329
CTRI/2021/01/030329尚未招募3 期

Comparative evaluation of post- operative pain after two irrigant activation techniques with Conventional Needle irrigation – A double blinded randomized controlled clinical trial

Sai Ram1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年1月18日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
150
试验地点
1
主要终点
Post operative pain after irrigation activation using VAS scale

研究概览

简要总结

The aim of the study is to compare the post- operative pain after the patients have been subjected to irrigant activation techniques at 6, 24 and 48 hours using visual analogue scale (VAS) from 0-10 and to correlate the intensity of pain and analgesic intake in patients with severe pain. Healthy patients in the age group of 18-65 years of age with symptomatic irreversible pulpitis and pain score from moderate to severe on VAS scale were included in the study. Patients who had analgesic within the last 12 hours were excluded from the study and immunocompromised patients, patients with calcified canal or periodontal disease were excluded from the study. The groups analyzed were conventional needle irrigation, Passive ultrasonic irrigation and Laser activated irrigation. The parameters evaluated were post operative pain after 6, 24 and 48 hours using VAS scale. The correlation between quantity and duration of analgesic intake in patients with severe pain were also evaluated after 24 hours.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Inclusion criteria Healthy patients Symptomatic irreversible pulpits Pain score ranging from moderate to severe 4-10 on VAS scale.

排除标准

  • Patients who had analgesic within last 12 h Systemic illness Drug allergy Pregnancy Lactation Calcified canal Periodontal disease.

结局指标

主要结局

Post operative pain after irrigation activation using VAS scale

时间窗: After 6, 24, 48 hours

次要结局

  • To assess the correlation between Post operative pain and Analgesic intake in Patients with Symptomatic Irreversible Pulpitis(After 24 hours)

研究者

发起方
Sai Ram
申办方类型
Research institution

研究点 (1)

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