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临床试验/NCT04988776
NCT04988776已完成1 期

Comparison Between Ultrasound-guided Pectoral Nerves Block Type II and Intercostobrachial Nerve Block as a Supplement to Supraclavicular Block for Anesthesia of Proximal Arteriovenous Access in End-stage Renal Disease Patients

Menoufia University2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年2月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
2
主要终点
intraoperative local anesthetic requirement

研究概览

简要总结

Brachial plexus block (BPB) is often utilized for proximal arm arteriovenous access creation. However, the medial upper arm and axilla are often inadequately anesthetized, as the Intercostobrachial nerve (which provides sensory supply to the axilla, upper medial arm, and a small area at the upper lateral chest) is not a component of the brachial plexus. This requires repeated, an intraoperative local anesthetic (LA) supplementation up to conversion into GA. The intercostobrachial nerve (ICBN) is a purely sensory nerve that arises primarily from the second intercostal nerve (T2) with occasional contribution from T3. Therefore, It is not a component of the brachial plexus and is not anesthetized by brachial plexus blockade. The ICBN can be blocked together with other nerves, such as the pectoral, intercostal, and long thoracic nerves in a recently described technique named pectoral nerves block type II (PECS II ).In this thesis, investigators compared the use of the PECS II block and ICBN block as a supplement to supraclavicular brachial plexus block for providing complete anesthesia of the upper arm for fistula creation surgery.

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 (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ESRD patients.
  • Proximal Arm Arteriovenous Access Surgery.
  • Elective or emergency surgery
  • American Society of Anesthesiology (ASA) physical status II to III.

排除标准

  • Inability of the patient to provide informed consent, communicate or cooperate
  • History of allergy to local anesthetics.
  • Preexisting upper limb neurological disease at the side of the surgery.
  • Patients on anticoagulant therapy or with history of coagulopathy.
  • Previous surgery at or near the site of the study.
  • The presence of skin infection at the puncture site.

结局指标

主要结局

intraoperative local anesthetic requirement

时间窗: 1-2 hours after surgery start

volume of local anesthetic

次要结局

  • postoperative pain(24 hours after end of surgery)

研究者

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

ashraf magdy eskandr

assistant professor of anesthesia

Menoufia University

研究点 (2)

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