跳至主要内容
临床试验/NCT06191445
NCT06191445尚未招募不适用

Does the Use of Ultrasound Increase Spinal Anesthesia Success for Obese Patients?: Evaluation of the Success of Spinal Anesthesia Administered with Real-Time Ultrasound-Guided, Ultrasound-Assisted and Conventional Landmark Techniques

Uludag University2 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2024年11月15日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
126
试验地点
2
主要终点
Success rates on the first attempt.

研究概览

简要总结

Spinal anesthesia is frequently administered using the conventional landmark technique. Ultrasound is a non-invasive and safe approach. Neuroaxial anesthesia procedures can be conducted using two different ultrasound techniques; Real-Time Ultrasound Guided (USRTG) and Ultrasound-Assisted (USAS). The primary objective of this study is to compare the successes of spinal anesthesia applications using USRTG, USAS, and conventional landmark techniques on the first attempt in obese patients undergoing orthopedic surgery.

详细描述

Patients included in the study will be those undergoing lower extremity orthopedic surgery, with a body mass index (BMI) 30 kg/m² and above, and classified as American Society of Anesthesiologists (ASA) class I-III. Patients will be randomized into 3 groups. In the Conventional Landmark group, spinal anesthesia will be administered using the conventional technique. In the Ultrasound-Assisted group, the spinal space will be marked with ultrasound before proceeding. For the Real-Time Ultrasound-Guided group, the spinal space and the advancement of the needle for the injection will be visualized simultaneously with ultrasound during the application of spinal anesthesia. The primary outcome is to compare the success rates on the first attempt. The secondary outcomes are to compare the number of skin punctures, needle redirections, procedure times, complications, and patient satisfaction

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 (Participant, Care Provider, Outcomes Assessor)

入排标准

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

入选标准

  • 18 years and older
  • Patients who will undergo lower extremity orthopedic surgery
  • ASA I-II-III patients
  • BMI 30 kg/m² and above

排除标准

  • BMI < 30 kg/m²
  • ASA IV-V patients
  • Severe cardiovascular disease
  • Patients with a known or suspected allergy to local anesthetics
  • Contraindications of spinal anesthesia (eg, coagulopathy, puncture site infection)

结局指标

主要结局

Success rates on the first attempt.

时间窗: Preoperatively

The primary outcome is to compare the success rates on the first attempt.

次要结局

  • Number of skin punctures, needle redirections, procedure times, complications, and patient satisfaction(Preoperatively)

研究者

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

Selcan Akesen

Associate Professor

Uludag University

研究点 (2)

Loading locations...

相似试验

Comparison of the Efficacy of Conventional Landmark,... | 临床试验