跳至主要内容
临床试验/CTRI/2026/01/101118
CTRI/2026/01/101118尚未招募不适用

Comparison of Ultrasound guided versus conventional method for difficult peripheral intravenous cannulation in adult population

Dr Bhawna Bansal1 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2026年1月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
128
试验地点
1
主要终点
success rate of intravenous cannulation on first attempt at the time of presentation in emergency

研究概览

简要总结

Comparison of Ultrasound-Guided versus Landmark Method for Difficult Intravenous Cannulation in Adult Population

Peripheral intravenous  cannulation is one of the most commonly performed procedures in emergency departments. However, it can be particularly challenging in patients with difficult venous access, leading to multiple failed attempts, patient discomfort, delayed treatment, and increased complications. Traditionally, landmark-based techniques are used to identify suitable veins, but these can be unreliable in difficult access cases due to factors such as obesity, edema, chronic illness, or previous IV drug use.

This prospective, randomized controlled study aims to compare the efficacy and safety of ultrasound-guided versus conventional landmark-based methods for peripheral IV cannulation in adults with difficult venous access in the emergency department. Eligible participants with predefined criteria for difficult IV access will be randomized into two groups one undergoing ultrasound-guided cannulation and the other using the standard landmark technique.

The primary objective is to compare the success rate of cannulation on the first attempt between the two groups. Secondary objectives include comparison of time taken for successful cannulation, number of attempts required, patient-reported pain score, and incidence of complications such as infiltration or hematoma.

The findings of this study may support broader implementation of ultrasound guidance in routine emergency care to improve success rates and patient outcomes.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 85.00 Year(s)(—)
性别
All

入选标准

  • A-DIVA score more than 3.

排除标准

  • 1 .patients not giving consent
  • pregnant and lactating mothers
  • very sick patients during presentation requiring central line access.

结局指标

主要结局

success rate of intravenous cannulation on first attempt at the time of presentation in emergency

时间窗: success rate of intravenous cannulation on first attempt at the time of presentation

次要结局

  • 1 number of attempts required for successful cannulation(2 time taken for successful cannulation)

研究者

发起方
Dr Bhawna Bansal
申办方类型
Other [(self)]
责任方
Principal Investigator
主要研究者

Dr Bhawna bansal

ABVIMS and Dr Ram Manohar Lohia hospital

研究点 (1)

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