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临床试验/CTRI/2026/01/102112
CTRI/2026/01/102112尚未招募3 期

Comparison of Ultrasound-Guided Posterior Tibial Artery Cannulation in Supine Versus Prone Position in Adult Surgical Patients : A Randomised Controlled Trial

All India Institute of Medical Sciences Jodhpur1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2026年2月6日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
180
试验地点
1

研究概览

简要总结

This prospective, randomized controlled trial aims to compare the effectiveness of ultrasound-guided posterior tibial artery (PTA) cannulation performed in the supine versus prone position in adult surgical patients requiring invasive arterial blood pressure monitoring. Eligible patients will be randomly allocated in a 1:1 ratio to either the supine or prone group using computer-generated block randomization with allocation concealment.

The primary outcome is the first-attempt success rate of PTA cannulation. Secondary outcomes include arterial diameter, ultrasound assessment time, cannulation time, total procedure time, number of attempts, complication rates, and operator-reported ease of cannulation. Outcomes will be assessed during and immediately after the procedure by a blinded outcome assessor.

The findings of this study are expected to help identify the optimal patient positioning for ultrasound-guided PTA cannulation, thereby improving procedural efficiency, safety, and clinical practice in perioperative and critical care settings.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Age 18–60 years
  • Scheduled for elective surgery requiring prone positioning
  • Requiring intra-arterial blood pressure monitoring
  • Palpable posterior tibial artery preoperatively
  • Written informed consent obtained.

排除标准

  • BMI > 30 kg/m²
  • Local infection, cellulitis, or wound near the cannulation site, trauma to the medial ankle, cannulation in the same artery/site
  • History of peripheral arterial disease
  • Previous surgery
  • PTA could not be visualised or appear thrombosed during initial scan.

研究者

发起方
All India Institute of Medical Sciences Jodhpur
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Sudip sikdar

All India Institute of Medical Sciences, Jodhpur

研究点 (1)

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