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临床试验/NCT05771935
NCT05771935已完成不适用

Ultrasound Guided Ulnar Versus Radial Artery Cannulation in Pediatrics Undergoing Major Non Cardiac Surgery: Double Blinded Randomized Controlled Study

Kasr El Aini Hospital2 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2023年3月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
112
试验地点
2
主要终点
Rate of successful cannulation at first attempt

研究概览

简要总结

This study aims to assess the safety and efficacy of ulnar artery cannulation compared to radial artery cannulation in pediatrics undergoing major non cardiac procedures.

详细描述

The study is a double blinded randomized controlled trial that will be conducted at Abu Al Reesh Children's Hospital, Faculty of Medicine, Cairo University after approval of research and ethics committees.

Children will be recruited into the trial during pre-operative assessment. will be randomly assigned to one of two groups Recruited patients will be randomly allocated by a computer-generated sequence of codes using randomization software (https://www. randomizer.org) into one of the two groups; in a 1:1 ratio (Group R) to receive radial artery cannulation and (Group U) to receive ulnar artery cannulation using ultrasound. The randomization sequence will be concealed in sequentially numbered, sealed opaque envelopes. The sealed envelopes will be opened by an anesthesia nurse immediately before induction of anesthesia.

After induction of anesthesia, modified Allen's test will be done by the ultrasound operator as following:

An Esmarch bandage will be used to exsanguinate the selected hand for cannulation according to the operator preference for 30 seconds, then the operator will apply simultaneous pressure to the ulnar and radial arteries of the chosen limb to occlude them. The bandage will then be released. Next, the pressure over the opposed artery selected for cannulation will be released and the time (in seconds) it takes for color to return to the hand will be measured.

Allen test results will be interpreted as follows:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
1 Month 至 10 Years(Child)
性别
All
接受健康志愿者

入选标准

  • - All pediatrics ASA I&II aged 1 month -10 years undergoing major non cardiac surgeries.

排除标准

  • • Patients undergoing cardiac surgeries.
  • Refusal of parents.
  • Ischemia defined as (color changes: blanching, duskiness, and or change in temperature of the extremity used for cannulation compared to the contralateral one).
  • Previous arterial cannulation within last week.
  • Patients requiring inotropic support before the start of procedures.
  • Rash or signs of infection or hematoma at the site of cannulation.
  • Patients requiring emergency procedures.

研究组 & 干预措施

(Group R)

Experimental

receive radial artery cannulation using ultrasound

干预措施: ultrasound guided radial versus ulnar artery cannulation (Procedure)

(Group U)

Active Comparator

receive ulnar artery cannulation using ultrasound

干预措施: ultrasound guided radial versus ulnar artery cannulation (Procedure)

结局指标

主要结局

Rate of successful cannulation at first attempt

时间窗: 15 minutes

(the procedure will be classified as successful when the artery is cannulated, and an arterial waveform is recorded within less than 3 attempts and or 15 minutes from the first puncture).

次要结局

  • diameters of the arteries after cannulation(15 minutes from start of cannulation)
  • incidence of vasospasm(15 minutes from start of cannulation)
  • diameters of the arteries before cannulation(preoperative)

研究者

发起方
Kasr El Aini Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Khaled Abdelfattah Abdallah Sarhan

principal investigator,Lecturer of anesthesia, Cairo university

Kasr El Aini Hospital

研究点 (2)

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