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临床试验/NCT07253961
NCT07253961尚未招募不适用

The Effects of Lateral Neck Cold Application for Vagal Nerve Stimulation on Pain During Peripheral Venous Cannulation in Obese Patients: A Prospective Randomized Controlled Study

Istinye University1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2025年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
150
试验地点
1
主要终点
Venous cannulation pain (VAS, 0-10)

研究概览

简要总结

This prospective, randomized controlled clinical trial aims to evaluate the effect of lateral neck cold application for vagal nerve stimulation on pain perception during peripheral venous cannulation in obese patients. Venous cannulation is a routine but painful procedure, especially in individuals with a body mass index (BMI) greater than 30, who often have heightened pain sensitivity due to chronic inflammation.

Participants will be randomly assigned to one of two groups:

Group 1 (Cold Application Group): A cold marble stone (0-4°C) will be applied to the lateral neck region (over the sternocleidomastoid muscle) for 5 seconds immediately before venous cannulation.

Group 2 (Control Group): Standard venous cannulation will be performed without any prior intervention.

Pain intensity will be assessed using the Visual Analog Scale (VAS) immediately after cannulation. Hemodynamic parameters (heart rate, blood pressure, oxygen saturation, respiratory rate) will be recorded before and after the procedure.

The primary outcome is the difference in VAS scores between the two groups. Secondary outcomes include changes in hemodynamic parameters. The study will enroll 150 participants over approximately two months following ethics approval.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 72 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults aged 18-72 years
  • •physical status I-III
  • •Scheduled for elective surgery
  • •Body Mass Index (BMI) > 30 kg/m²
  • •Provided written informed consent

排除标准

  • •Emergency surgical cases
  • •Oncologic surgery
  • •Pregnant patients
  • •History of hand dorsum surgery or scarring
  • •Psoriasis or other local skin lesions/infections at cannulation site
  • •Peripheral vascular disease
  • •Chronic analgesic, opioid, steroid, or gabapentinoid use
  • •Substance abuse history
  • •Peripheral neuropathy
  • •Previous or ongoing oncologic treatment
  • •Severe mental retardation or communication impairment preventing cooperation

研究组 & 干预措施

Cold Application Group

Experimental

Participants will receive cold stimulation to the lateral neck region (over the sternocleidomastoid muscle) using a marble stone cooled to 0-4°C for 5 seconds immediately before peripheral venous cannulation.

干预措施: Cold Application to Lateral Neck Region (Procedure)

Standard Venous Cannulation Group

Placebo Comparator

Participants will undergo routine peripheral venous cannulation without any prior intervention.

干预措施: Cold Application to Lateral Neck Region (Procedure)

结局指标

主要结局

Venous cannulation pain (VAS, 0-10)

时间窗: Immediately after cannulation (within ~1 minute)

Pain intensity will be assessed once, right after peripheral venous cannulation, using a 10-cm Visual Analog Scale (0 = no pain, 10 = worst imaginable pain). The score will be recorded as a continuous variable and compared between groups.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

İlke Dolgun

Assoc. prof

Istinye University

研究点 (1)

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