EUCTR2015-002381-23-FR进行中（未招募）1 期
Comparison of the efficacy of IV paracetamol and IV ketoprofen in the treatment of renal colic in emergency department : a two-center double blind randomized study. - PIVKIV
CHU de Nîmes0 个研究点开始时间: 2015年9月11日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •informed consent
- •The patient is available for telephone follow-up to one week
- •The patient is at least 18 years old.
- •suspected renal colic
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 338
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 338
排除标准
- •The patient has contreindication for a necessary treatment in this study.
- •The patient has an allergy to ketoprofen or paracetamol , of gastric or intestinal ulcer , bleeding disorders, a history of asthma triggered by taking ketoprofen or similar activity substances
- •The patient has hyperthermia, hemodynamic instability, oligoanuria .
- •The patient has an initial pain assessed by NRS 10/10 .
- •The patient has a history of aneurysm or aortic dissection, kidney transplant , single kidney, liver or kidney failure .
- •ketoprofen or paracetamol administration four hours before treatment to emergencies.aracétamol 4 heures avant le traitement en structure d'urgence.
研究者
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