IRCT20220407054442N1已完成2 期
Comparison of prophylactic effect of single-dose Celecoxib and Mefenamic acid in reducing pain after tooth extraction
Shahre-kord University of Medical Sciences0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 14 years 至 no limit（—）
- 性别
- All
入选标准
- •Patients over 14 years and of any sex who do not have a serious systemic disease and are classified in class 1 or 2 of The American Society of Anesthesiologists (ASA) will be included in this study.
排除标准
- •Patients who referred for tooth extraction due to periodontal support problem will not be included in the study.
- •Patients with symptoms of infection such as swelling, fever, pus discharge, and decreased mouth opening will also not be included in the study.
- •Patients who need analgesics for any reason other than toothache will not be included in the study.
- •Patients who have a history of taking any painkillers up to 12 hours before tooth extraction will not be included in this study.
- •Patients with systemic physical or mental illness or at risk for infectious endocarditis, coagulation problems, local and systemic infections, known allergies to celecoxib or mefenamic acid, a history of asthma, or drug or alcohol addiction will not be included in this study.
- •Patients who require severe surgical intervention to extract a tooth will not be included in this study.
- •celecoxib is contraindicated in patients with heart problems. Therefore, patients with heart disease will not participate in this study.
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