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临床试验/NCT04311255
NCT04311255已完成3 期

Comparing the Efficacy and Safety of Ultrasound Guided Supraclavicular Block Combined With Either Intercosto-brachial Nerve Block or pec11block for Creation of Surgical Brachio-basilic Fistula in Chronic Renal Failure Patients on Hemodialysis

Ain Shams University2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2019年4月13日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
4
试验地点
2
主要终点
the proportion of patients with adequate block (no need for intraoperative local infiltration),

研究概览

简要总结

In our study we are trying to reach to the more efficient us guided peripheral nerve block either intercosto-brachial or PPEC 11 that can be combined with us guided supraclavicular block to effectively anesthetise the surgical site for creation of brachio-basilic fistula as regarding onset of surgical anesthesia, adequacy of intra-operative anesthesia, the need for surgical wound infiltration, duration of postoperative analgesia and the failure rate of the fistulae.

详细描述

  • Type of Study: Randomized Prospective trail
  • Study Setting: Ain Shams University Hospitals, Cairo, Egypt
  • Study Period: 6 months.

Sampling Method: Patients will be subdivided randomly into two groups :

Group (SI) : 25 ml of bupivacaine 0.5 % for us guided supraclavicular block plus 10 ml of lidocaine 2% for us guided intercostobrachial nerve block.

Group(SP) : 25 ml of bupivacaine 0.5 % for us guided supraclavicular block plus10 ml of lidocaine 2% for us guided PECll block.

Study Procedures:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • American Society of Anesthesiologists Grade III, age 25-75 years who are scheduled for brachio-basilic AVF.

排除标准

  • Patients will be excluded if they have infection at the injection site, allergy to local anesthetics, chronic use of opioids, a history of neurological neuromuscular, or severe hepatic or cardiopulmonary disease, a contraindication to regional anesthesia or patient /guardian refusal.

结局指标

主要结局

the proportion of patients with adequate block (no need for intraoperative local infiltration),

时间窗: "through study completion ,an average of one year"

ratio

次要结局

  • duration of postoperative analgesia("through study completion ,an average of one year")
  • onset of surgical anesthesia("through study completion ,an average of one year")
  • the failure rate of the fistulae.("through study completion ,an average of one year")

研究者

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

Amira Fathy Hefni,MD-EDIC

Assistant professor

Ain Shams University

研究点 (2)

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