NCT03314948终止不适用
Ultrasound-Guided Costoclavicular Block in Patients With a BMI > 30
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- Mayo Clinic
- 入组人数
- 2
- 试验地点
- 1
- 主要终点
- Success rate of costoclavicular brachial plexus block
研究概览
简要总结
The Researchers are trying to determine if Costoclavicular brachial plexus block (CCBPB) can be successfully performed in patients with a body mass index greater than thirty.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •18 to 80 years old, with American Society of Anesthesiologists physical status I to IV, undergoing elective hand or forearm surgery under a BPB will be enrolled for this study.
排除标准
- •Patient's refusal, American Society of Anesthesiologist physical status greater than IV, pregnancy, neuromuscular disease, prior surgery on the intraclavicular fossa, nerve injury or neurological disorders, bleeding tendency or evidence of coagulopathy, history of allergy to local anesthetic drugs, skin infection at the site of needle insertion, or contraindication to regional anesthesia.
结局指标
主要结局
Success rate of costoclavicular brachial plexus block
时间窗: Within 45 minutes of completion of block placement
Determine the success rate of the block in patients with body mass index greater than 30. Assess the effectiveness of the block by performing required assessments
次要结局
- Identification of costoclavicular space(during placement of the block)
研究者
Christopher B. Robards
Principal Investigator
Mayo Clinic
研究点 (1)
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