Ultrasound Guided Peribulbar Anaesthesia: a Real-time Ultrasound Guided Technique With a Novel Dual Quadrant Injection
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 22
- 主要终点
- Block Success
研究概览
简要总结
Peribulbar anaesthesia for ocular surgery depends on the spread of local anaesthetic throught the orbit to be successful and has a relatively high failure rate. This study will examine a novel ultrasound guided approach to peribulbar anaesthesia which should extend the depostion of local anaesthetic by using a dual quadrant injection technique. The study will assess the feasibility of this technique, how successful it is and whether any obvious safety issues arise with its use.
详细描述
Peribulbar anesthesia is widely used for anterior and posterior chamber ophthalmic procedures. It is a blind technique which is traditionally carried out by inserting a needle in the infero-lateral aspect of the orbit below the globe and injecting a volume of 8 - 12 mL of local anesthetic in the periorbital space. The goal of this inejction is to achieve akinesia and anesthesia of the eye sufficient for surgery. The technique has a relatively high failure rate of up to 30%. A failure or insufficient block requires a second or rarely a third peribulbar injection to achieve success. Ultrasound can be used to guide needles in the human body and has been successfully used in many anatomic locations for anaesthesia. This study will assess whether ultrasound can guide the block needle in ophthalmic anesthesia to deliver local anesthetic via a single entry into two discrete locations within the periorbital space - the first in the infero-lateral quadrant and the second in the infero-medial quadrant. If this can be done the investigators may achieve a higher success rate for this block with a lower volume potentially improving the quality of the block and its safety.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 90 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •ASA score less than III and ability to provide a written informed consent
- •22 patients presenting for opthalmic surgery
排除标准
- •Coagulation disorder or anticoagulated with INR > 1.5
- •Platelet count < 75 X 10*9/L
- •Significant Myopia (axial length > 28mm)
- •Patients unable to lie supine for 2 hours
- •Patients with recent gas or silicone injections in/around the eye
结局指标
主要结局
Block Success
时间窗: 10 minutes post intervention
Block will be deemed a failure if a supplementary block is required for the operative procedure
次要结局
- Block Quality (standardized Ocular Scoring System for akinesia and anaesthesia)(5 and 10 minutes)
- Duration of Procedure(1 to 10 minutes)
- Complications(6 Weeks)
- Image Visualization(1 minute)
- Block Volume(1 minute)
