CTRI/2021/04/033256已完成不适用
Comparative evaluation of the effectiveness of intracanal and intraoral cryotherapy on postendodontic pain in patients with symptomatic apical periodontitis: A randomized clinical trial.
DR AJEESH K1 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2021年2月6日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 108
- 试验地点
- 1
- 主要终点
- Pain measurement using Visual Analog Scale after Root Canal Treatment
研究概览
简要总结
This study is a randomized, double-blinded, parallel group clinical trial to assess and compare the effectiveness of intracanal and intraoral cryotherapy on postoperative pain in teeth with symptomatic apical periodontitis. The primary outcome measure will be the measurement of postoperative pain in intracanal, intraoral and control group, 6 and 24 hours postoperatively using Visual Analog Scale. The secondary objectives are the measurement of the need for analgesics and postoperative pain changes among gender and age groups.
研究设计
- 研究类型
- Interventional
- 分配方式
- Permuted block randomization, fixed
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 55.00 Year(s)（—）
- 性别
- All
入选标准
- •1.Uniradicular teeth that are diagnosed with symptomatic apical periodontitis.
- •2.Healthy patients without systemic disease.
- •3.Patients with pre-operative pain score ranging from moderate to severe (3–10) on a visual analog scale (VAS) (0–10).
排除标准
- •1.Pregnant patients 2.Patients with severe periodontal diseases 3.Teeth with incomplete apex formation, excessively curved roots and calcified canals 4.Periapical abscess and sinus opening 5.Patients on analgesics for the last 8 hours or on antibiotic therapy.
- •6.Previous root canal treatment.
- •7.Cases with broken files, over-instrumentation.
结局指标
主要结局
Pain measurement using Visual Analog Scale after Root Canal Treatment
时间窗: 6 and 24 hours postoperatively
次要结局
- Need for analgesic usage(6 and 24 hours postoperatively)
- Pain changes among gender and age groups(6 and 24 hours postoperatively)
研究者
研究点 (1)
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