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临床试验/NCT06074471
NCT06074471招募中不适用

Motor Sparing Supraclavicular Brachial Plexus Block (MS-SCBPB): A Randomized Controlled Trial

Cairo University2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2023年9月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
44
试验地点
2
主要终点
Duration of motor blockade

研究概览

简要总结

This study aims to compare MS-SCBPB and SCBPB in the duration of postoperative analgesia, time to first analgesic request (VAS ≥40 mm), pain scores, motor power, and side effects.

详细描述

On arrival of the patients to regional anesthesia room, patients will be secured with 20-gauge intravenous cannula. Monitoring will include ECG, non-invasive arterial blood pressure, and pulse oximetry (SpO2).

Before receiving supraclavicular brachial plexus block, patients will be randomly assigned into one of the two study groups:

MS-SCBPB Group (n=22): this group will receive ultrasound-guided supraclavicular brachial plexus block with total volume 20 mL bupivacaine 0.20% and 8 mg dexamethasone.

SCBPB Group (n=22): this group will receive ultrasound-guided supraclavicular brachial plexus block with total volume 20 mL bupivacaine 0.5% and 8 mg dexamethasone.

Another doctor not involved in the block procedure will evaluate the patients postoperative.

研究设计

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

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

  • Patients scheduled for upper limb surgeries under supraclavicular brachial plexus block
  • American Society of Anesthesiologists (ASA) status I and III
  • between ages of 18 and 60 years

排除标准

  • Bleeding disorders with INR > 1.5 and/or platelets < 100,000/mm3
  • infection at the injection site
  • Allergy to local anesthetics
  • Severe cardiopulmonary disease (≥ASA IV)
  • Diabetic or other neuropathies
  • Motor disorders
  • Patients receiving opioids for chronic analgesic therapy
  • Inability to comprehend visual analogue scale (VAS).

结局指标

主要结局

Duration of motor blockade

时间窗: 24 hours

Duration of motor blockade

次要结局

  • Time to first analgesic request(24 hours)
  • Total morphine requirements(24 hours)
  • Visual analogue scale (VAS)(24 hours)
  • Time needed for complete recovery from sensory and motor block at 2, 4, 6, 12, 18, and 24 hours postoperatively.(24 hours)
  • Time needed for surgical block:(24 hours)

研究者

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

Nagy Malak , MD

Lecturer of anesthesia ,SICU and pain

Cairo University

研究点 (2)

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