跳至主要内容
临床试验/NCT05706090
NCT05706090已完成不适用

Effect of Neurostimulator Usage on Block Success in Costoclavicular Block: a Randomized Controlled Trial

Gaziosmanpasa Research and Education Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年2月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
The block success rate (ratio of successful blocks to all blocks)

研究概览

简要总结

The need of a neurostimulator for a successful nerve block was questioned in different block types after ultrasound has become standard. The aim of this clinical study was to determine the effect of neurostimulator use on block success in costoclavicular block

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Class I, II and III of American Society of Anesthesiologists (ASA) classification
  • being between 18 and 80 years of age,
  • body mass index (BMI) between 18 and 35 kg/m2

排除标准

  • Patients who did not give consent,
  • were above ASA III,
  • pregnant,
  • had a neuromuscular disease,
  • bleeding diathesis,
  • a local anesthetic allergy,
  • an infection in the area where nerve block would be applied, and
  • had previously operated from the infraclavicular fossa were not included in the study

研究组 & 干预措施

Group USP

Experimental

The group using ultrasound and injection pressure manometer was named USP

干预措施: fentanyl will be added (Drug)

Group USP

Experimental

The group using ultrasound and injection pressure manometer was named USP

干预措施: general anesthesia (Procedure)

Group USPN

Experimental

The group using ultrasound , injection pressure manometer , and neurostimulator was named USPN

干预措施: fentanyl will be added (Drug)

Group USPN

Experimental

The group using ultrasound , injection pressure manometer , and neurostimulator was named USPN

干预措施: general anesthesia (Procedure)

结局指标

主要结局

The block success rate (ratio of successful blocks to all blocks)

时间窗: during procedure

The block was considered unsuccessful in case of analgesic need during the surgery or transition to general anesthesia, otherwise, these patients were included in the successful block group.

次要结局

  • time to readiness for surgery(30 minutes)
  • Block application time(30 minutes)
  • number of needle passes(30 minutes)

研究者

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

Döndü Genc Moralar

Associate Professor

Gaziosmanpasa Research and Education Hospital

研究点 (1)

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