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临床试验/IRCT2015061622768N1
IRCT2015061622768N1已完成1 期

Randomized clinical trial of the comparison of splinting/non splinting in prevention of superficial phlebitis following Amiodarone Injection in patients with Cardiac Arrhythmia

Tehran University of Medical Sciences, Vice Chancellor For Research0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
60

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
18 years 至 65 years(—)
性别
All

入选标准

  • •1- Age between 18 and 65 years
  • •2- Amiodarone administration for atrial fibrillation or ventricular tachycardia
  • •3- Starting dose of Amiodarone administration at CCU
  • •4- Informed consent of the patient regarding the use of the splint. In case of the patient’s incapacity, informed consent will be obtained from the patient’s first-degree relatives (e.g., parents). The patients will be reassured that their treatment course will not be affected by non-participation in the study.
  • •Exclusion criteria:
  • •1- History of cancer and chemotherapy, deep vein thrombosis, renal failure and dialysis, consumption of broad-spectrum antibiotics and steroids
  • •2- Removal of the splint in consequence of the patient’s agitation
  • •3- Refusal to give consent for participation in the study

排除标准

  • 未提供

研究者

发起方
Tehran University of Medical Sciences, Vice Chancellor For Research

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