跳至主要内容
临床试验/PACTR202402842689533
PACTR202402842689533招募中Unknown

Cervical Erector Spinae Plane Block versus Posterior Interscalene Brachial Plexus Block in Patients Undergoing Shoulder Arthroscopy: A Prospective Randomised Parallel Trial

未提供0 个研究点目标入组 80 人开始时间: 2024年1月16日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • Patients aged 18–65 years
  • American Society of Anesthesiologists (ASA) I or II
  • Scheduled for elective unilateral shoulder arthroscopy (rotator cuff repair, bankart repair, superior labral tear from anterior to posterior repair, and/or acromioplasty).

排除标准

  • Coagulation Or bleeding disorder, anticoagulant therapy
  • Cervical disc issues,
  • Allergy/sensitivity to local anaesthetics and/or opioids,
  • Infection in the block area,
  • Contralateral hemidiaphragmatic paralysis, pneumonectomy or vocal cord palsy, severe bronchopulmonary disease, including chronic obstructive pulmonary disease and obstructive sleep apnea.
  • Pregnancy or suspected pregnancy, breast feeding mother,
  • Body mass index greater than 35 kg/m2,
  • Significant psychiatric or cognitive conditions interfering with assessment.
  • Unstable coronary artery disease, congestive heart failure, or arrhythmias.
  • Pre-existing neurological deficits or neuropathy affecting the brachial plexus. Cognitive or intellectual disability resulting in difficulty communicating with the care givers.
  • Pre-existing chronic pain or daily consumption of opioid analgesics.
  • Significant renal or hepatic impairment.
  • Refusal to participate
  • Block failure

研究者

发起方
未提供

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