CTRI/2021/04/032814尚未招募不适用
The effect of novel rotary file systems along with irrigation agitation technique on postoperative pain in teeth with symptomatic irreversible pulpitis : a randomized clinical trail
Dr Ravuri Varshini Meghana1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2021年1月11日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Assessment of post-operative Pain scores using Visual Analog Scale
研究概览
简要总结
This is a randomized, double blind, parallel group, single center trial in which we compare the effect of anatomical rotary and conventional rotary file systems along with manual dynamic agitation on post-operative pain in patients with symptomatic irreversible pulpitis will be assessed using Visual Analog Scale[VAS] at 6,24,48,and 72 hours andon 7th day.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 50.00 Year(s)(—)
- 性别
- All
入选标准
- •Patients with symptomatic irreversible pulpitis in posterior teeth.
- •Healthy patients of age group between 18-50 yrs.
- •Patients with preoperative pain scores which will vary from moderate to severe pain on a visual analog scale(VAS).
- •Patients who will have the ability to understand and to use the pain scale.
排除标准
- •Patients with pain on percussion Patients with traumatic occlusion, severe malocclusion Teeth with calcified canals Teeth with periapical radiolucency Teeth with root resorption Teeth with immature open apex Patients with Re -RCT will be excluded.
- ••Patients who has taken analgesic or anti-inflammatory drugs within the last 12 hour •Patients with known allergy to local anesthesia, sodium hypochlorite and chlorhexidine.
- •Presence of systemic diseases like cardiovascular disease, renal disease, bleeding disorders or any anti-coagulant use with in last month.
- •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
Assessment of post-operative Pain scores using Visual Analog Scale
时间窗: at 6,24,48,and 72 hours and on 7th day
次要结局
- assessing quality of life using OHIP 14 criteria(at 72 hours)
研究者
研究点 (1)
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