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临床试验/NCT03376308
NCT03376308已完成不适用

Evaluation of the Effect of Venous Diameter Measurement by Ultrasonography on Pain and Withdrawal Response

Aydin Adnan Menderes University1 个研究点 分布在 1 个国家目标入组 145 人开始时间: 2017年6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
145
试验地点
1
主要终点
The injection pain due to propofol

研究概览

简要总结

During general anesthesia, intravenous (IV) medications can disrupt the patient's comfort by causing a pain sensation or a withdrawal response in the heart. Propofol and rocuronium are among the most common causes of this condition.

In recent years, the use of ultrasonography (USG) in anesthesia has become widespread with the rapid advancement of technology. The use of the patient's head is a non invasive method.

This study is aimed to evaluate whether the size of the venous diameter assessed by ultrasonography in our study is an effect on pain and withdrawal response after drug injections.

详细描述

The study was conducted in patients who underwent surgical procedures under general anesthesia by obtaining consent from the Adnan Menderes University Medical Faculty Ethics Board and written consent from the patients and then being admitted to the ASA I-II age group 18-70 years of age.

Patients with peripheric vascular disease, vasculitis, rheumatologic disease, non-cooperative, under the age of 18 and over 70, ASA III and above, allergic to general anesthetic agents and refusing to participate in the study were excluded from the study.

研究设计

研究类型
Observational
观察模型
Case Crossover
时间视角
Prospective

入排标准

年龄范围
17 Years 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18- 70 years of ASA (American society of anesthesiology) physical status I- II who were to undergo various elective operations

排除标准

  • Rheumatologic disease Peripheric vascular disease Vasculitis Patients with chronic pain syndrome, Patients with neurologic deficits, Patients with thrombophlebitis, Patients with difficult venous access, Patients with allergy

结局指标

主要结局

The injection pain due to propofol

时间窗: 6 month

Pain will be recorded and graded using a 4-point scale (none, mild, moderate, or severe).

次要结局

  • The withdrawal movement due to rocuronium(6 month)

研究者

发起方
Aydin Adnan Menderes University
申办方类型
Other
责任方
Principal Investigator
主要研究者

SİNAN YILMAZ

Principal Investigator

Aydin Adnan Menderes University

研究点 (1)

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