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临床试验/TCTR20201027002
TCTR20201027002尚未招募未知

Effect of dexamethasone or ibuprofen-acetaminophen combination for pain management in symptomatic apical periodontitis during COVID-19 outbreak: a retrospective cohort study

A0 个研究点目标入组 50 人开始时间: 2020年10月27日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
A
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
0 Years 至 65 Years(—)
性别
All

入选标准

  • 1) age, 18â€65 years, 2) maxillary\ mandibular molar tooth with symptomatic apical periodontitis and vital pulp, 3) the given medications were the same (ibuprofen 600 mg + acetaminophen 500 mg twice for 3 days or 4 mg dexamethasone twice for 1 day) and 4) complete clinical/radiographic data and pain levels at baseline, 6, 12, 18, 24, 48 and 72 hours.

排除标准

  • 1) necrotic pulp, 2) periapical index score 4 and 5 proposed by Ørstavik et al. [12], 3) pregnancy and systemic disease or allergic reactions, 4) sensitivity or adverse reactions to medicines, 5) taken any analgesics or anti-inflammatory drug within the last 3 days, 6) swelling or acute/chronic abscess, 7) active orthodontic appliances and 8) multiple carious teeth.

研究者

发起方
A

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