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临床试验/NCT02622269
NCT02622269已完成不适用

Patient-driven Compression in Urography

Örebro University, Sweden2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2015年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
2
主要终点
Radiation dose measured as Dose-area product

研究概览

简要总结

Compression of the abdomen during urography with either a patient-regulated compression device or conventional compression.

Evaluation of radiation dose, image quality and patients' experiences

详细描述

Patients are subjected to radiation from radiographical studies. The nurse can reduce the radiation dose for the individual by using dose-reducing measures. One of these is compression. It is known that compression in urography reduces the radiation dose because the radiation has less tissue to transverse when it is compressed. By reducing patient radiation doses, the risk of harmful radiation effects is reduced. This study aims to study if a patient-regulated compression device can reduce the radiation dose as effectively as the conventional compression, regulated by the nurse.

Two compression devices are investigated in each patient, in randomized order.

Aims of the study:

  1. Evaluate if the radiation doses are comparable with a patient-regulated compression device and conventional compression.
  2. Evaluate image quality with the two devices.
  3. Describe patients' experiences from using the two devices.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Outpatients with a request for a urographic study

排除标准

  • Emergency studies,
  • cannot participate actively with compression,
  • contraindications to compression of the abdomen,
  • pregnancy,
  • inability to understand the language of the questionnaire

结局指标

主要结局

Radiation dose measured as Dose-area product

时间窗: Immediately

Radiation dose for the investigated exposures, measured as Dose-area product

次要结局

  • Image quality measured with Visual Grading(Immediately)
  • Patient experience (questionnaire)(Immediately after the procedure)

研究者

发起方
Örebro University, Sweden
申办方类型
Other
责任方
Principal Investigator
主要研究者

Håkan Geijer

MD, PhD

Örebro University, Sweden

研究点 (2)

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