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
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