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临床试验/NCT07326436
NCT07326436已完成不适用

Comparison of Sympathetic Block Duration and Rebound Sympathetic Activity Rate in Infraclavicular and Supraclavicular Brachial Plexus Blocks Using Perfusion Index and Skin Temperature

Bozyaka Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2023年3月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200
试验地点
1
主要终点
Difference in duration of sympathetic blockade after different US-guided brachial plexus blocks

研究概览

简要总结

This prospective comparative study will evaluate the sympathetic effects of ultrasound-guided infraclavicular versus supraclavicular brachial plexus blocks in adults undergoing upper-extremity surgery. Sympathetic tone will be monitored noninvasively with simultaneous bilateral measurements of perfusion index (pulse-oximetry-derived) and skin temperature obtained at baseline and at predefined post-block intervals until return to baseline. The primary outcome is the duration of sympathetic block. Secondary outcomes are between-approach differences in the time course of perfusion index and skin temperature, and the incidence and magnitude of rebound sympathetic activity.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 to 65 year old
  • Patients scheduled for upper extremity surgery
  • Fully oriented and able to cooperate
  • Patients who signed the informed consent form and gave consent to participate in the study

排除标准

  • ASA III-IV-V
  • Non-cooperation
  • Disease that interferes with sensory block assessment
  • Known allergy to the medicines to be used
  • Pregnant patients
  • Coagulopathy or thrombocytopenia
  • Patients with anatomical abnormalities or active infection at the points of application

研究组 & 干预措施

Supraclavicular brachial plexus block

Active Comparator

干预措施: Supraclavicular brachial plexus block (Procedure)

Infraclavicular brachial plexus block

Active Comparator

干预措施: Infraclavicular brachial plexus block (Procedure)

结局指标

主要结局

Difference in duration of sympathetic blockade after different US-guided brachial plexus blocks

时间窗: Twenty-four hours after nerve blockage

次要结局

  • Change in perfusion index between infraclavicular and supraclavicular approaches(Twenty-four hours after nerve blockage)

研究者

发起方
Bozyaka Training and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Pelin Doğan Uzun

Doctor of medicine

Bozyaka Training and Research Hospital

研究点 (1)

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