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临床试验/NCT04921891
NCT04921891已完成不适用

Comparison of Block Success in Patients Undergoing Ultrasound-guided Infraclavicular Brachial Plexus Block With Bilateral Upper Extremity Perfusion Index

Bakirkoy Dr. Sadi Konuk Research and Training Hospital2 个研究点 分布在 2 个国家目标入组 30 人开始时间: 2014年4月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
2
主要终点
Evaluation of whether perfusion index is a reliable and objective method to indicate block success

研究概览

简要总结

The infraclavicular nerve block, which is frequently preferred in upper extremity surgeries, provides additional advantages such as reduction in opioid consumption by providing analgesic effect in the postoperative period as welll. The success of peripheral nerve blocks is usually assessed by subjective feedback from the patient, and patient cooperation is needed. The aim of this study is to assess whether the perfusion index level, which can be measured noninvasively, can be a predictor of the infraclavicular block success.

详细描述

Thirty patients who were operated on for carpal tunnel syndrome under infraclavicular brachial plexus block were included in our study. After the procedure, at 10-minute intervals, the sensory block was assessed by a pinprick test, and the motor block was assessed by the ability to flex the hand and the forearm. In addition, PI and skin temperature were measured 0-10-20-30 minutes after the block and at postoperative 2, 4, and 6 hours. 30 minutes after the measurements, the surgical procedure was allowed to begin in patients with successful block.

研究设计

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

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ages of 18-75
  • Patients who will diagnose with carpal tunnel syndrome by electroneuromyography (ENMG), and will undergo unilateral surgery under elective conditions
  • ASA I-II-III patients

排除标准

  • Patients who will refuse this method
  • Neurological deficits,
  • Diabetes mellitus,
  • Local anesthetic allergy,
  • Morbidly obese,
  • Peripheral vascular disease, coronary artery disease, or coagulopathy

结局指标

主要结局

Evaluation of whether perfusion index is a reliable and objective method to indicate block success

时间窗: 6 hours postprocedurly

Perfusion index was measured up to 6 hours after the procedure.

次要结局

  • Determining of a cut-off value for PI and PI ratio for a successful block.(Up to 6 hours after the procedure)

研究者

发起方
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Gokhan Sertcakacilar, MD

Principal investigator

Bakirkoy Dr. Sadi Konuk Research and Training Hospital

研究点 (2)

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