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临床试验/ACTRN12623000071628
ACTRN12623000071628已完成未知

The effect of fasting prior to non-emergency contrast-enhanced computed tomography on the incidence of non-ionic intravenous contrast-induced adverse reactions in adults: A randomised clinical trial

Fundación para la Investigación Biosanitaria en Andalucía Oriental (FIBAO)0 个研究点目标入组 1,148 人开始时间: 2023年1月23日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
1,148

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Patients must be scheduled for a non-emergency contrast-enhanced CT scan during weekdays and be equal to or older than 18 years in order to participate in the study.

排除标准

  • Incomplete form data filling, presence of intravenous contrast extravasation, intake of antiemetic and prokinetic medication 8 to 12 hours before the examination, patients with overt hyperthyroidism, history of allergic reaction or hypersensitivity to iodinated contrast media and patients unable to provide written informed consent.

研究者

发起方
Fundación para la Investigación Biosanitaria en Andalucía Oriental (FIBAO)

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