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临床试验/NCT01440400
NCT01440400已完成不适用

The Use of Ultrasound to Guide Spinal Anesthesia in Obstetrics. Is There an Advantage Over Landmark Technique in Non-obese Patients?

Corniche Hospital2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2011年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
150
试验地点
2
主要终点
The number of skin punctures

研究概览

简要总结

The classical method for spinal anesthesia relies on the use of bony landmarks to identify the level and point of entry of the spinal needle. Over the years, in experienced hands, this method consistently proved to be successful and safe.

The introduction of ultrasound to guide neuraxial anaesthesia into clinical practice was relatively slow compared to peripheral nerve blocks or central venous catheterization. This could be due to the technical difficulties posed by the bony structures surrounding the spinal cord and its dura that blocks the path of the ultrasound beam. Many anesthetists are reluctant to change their conventional landmark technique, particularly with most studies showing no change in the success rate between ultrasound guided and the landmark techniques.

Several studies however showed that the ultrasound guided approach reduces the number of attempts to achieve a successful block and reduces the procedure time particularly in obese patients and those with technical difficulties.

In this study the investigators are trying to answer the following question : Is there any advantage in using ultrasound to guide spinal anaesthesia in non obese obstetric patients with easily palpable bony landmarks?

详细描述

Patients will be randomized using a web based randomization program into two groups: Ultrasound guided spinal anesthesia (US) & conventional spinal anesthesia (C). In both groups, the level of the third or fourth lumbar inter-space (L3/4 or L4/5) will be identified using either ultrasound (transverse and longitudinal approach) or palpation method using anatomical landmarks.

All ultrasound examinations and spinal anesthesia will be performed by 3 anesthetists with experience in ultrasound guided neuraxial block (between 100 and 200 cases). The ultrasound examination will be done using Logiq e TM ultrasound machine (GE Solingen Germany) with 4C RS 2 - 5.5MHz Broadband multi-frequency probe.

The predetermined point of entry for the introducer needle will be marked on the patient's back. The spinal anaesthesia will be administered with the patient in the sitting position, using a 26 gauge pencil point needle (PortexTM) with 15 mg of heavy Bupivacaine and 20 micrograms of Fentanyl. An independent observer, who is blinded to the method used to identify the point of entry of the introducer needle, will be collecting the data.The spinal anesthesia will be labeled as successful if a bilateral block to the sixth thoracic dermatome (T6) , judged by loss of cold and touch discrimination, is established 5 minutes after the spinal injection.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single (Outcomes Assessor)

入排标准

性别
Female
接受健康志愿者

入选标准

  • All mothers with body mass index (BMI) equal to or less than 35 who has normal singleton pregnancy
  • At 37 weeks gestation or more
  • Admitted to Corniche Hospital for elective caesarean section under spinal anaesthesia

排除标准

  • Patients with BMI >35
  • Patieints with difficult anatomical landmarks
  • Patients with neurological disease or coagulation defects
  • Patients receiving anticoagulants
  • Patients refusing spinal anaesthesia

结局指标

主要结局

The number of skin punctures

时间窗: 30 minutes

Number of times the skin is punctured by the introducer needle.

The number of spinal needle passes

时间窗: 30 minutes

The number of times the spinal needle tip is advanced beyond the tip of the introducer needle.

The time of the procedure

时间窗: 30 minutes

From skin puncture by the introducer to viewing cerebro-spinal fluid back-flow at the hub of the spinal needle.

次要结局

  • The patient satisfaction with spinal anesthesia(24 hours)
  • Backache after spinal needle placement, assessed within 24 hours postoperatively(24 hours)

研究者

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

Dr. Tarek Ansari

Consultant anesthetist

Corniche Hospital

研究点 (2)

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