NCT01583179终止不适用
Duration of Analgesic Effect for Ultrasound Guided Supraclavicular Blocks With the Addition of Buprenorphine to Local Anesthetic Solution
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 26
- 试验地点
- 1
- 主要终点
- Time Until First Pain Medication Post-operatively
研究概览
简要总结
The patients included will be those who have already agreed to have a brachial plexus nerve block for surgery. A flip of the coin will decide who gets and additive called buprenorphine in their block or not. They will both contain the same amount and type of numbing medicine. The goal will be to see if the additive extends the life of the pain control portion of the ultrasound guided supraclavicular nerve block.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 79 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •American Society of Anesthesiologists (ASA) physical status 1-3
- •Age 18-79, inclusive
- •BMI <36 kg/m^2
- •Patient consenting to single injection brachial plexus nerve block as primary anesthetic for a procedure
排除标准
- •Patients with coagulation disorders
- •Clinically significant pulmonary disease
- •Clinically significant cardiac disease
- •Neurologic deficit in surgical extremity
- •Allergy to bupivacaine or buprenorphine
- •Intolerance of narcotics
- •Local infection over intended area of needle insertion
- •Hepatic failure or renal failure
- •Significant psychiatric disease, including drug abuse
- •Seizure disorder
- •Possible pregnancy or lactation by patient report
- •Use of narcotic medication greater than 2 times a week for greater than 1 week.
- •Patients for whom the surgeon requests a shorter-acting block
研究组 & 干预措施
buprenorphine
Experimental
will receive local anesthetic, epinephrine and the additive buprenorphine to nerve block
干预措施: Buprenorphine (Drug)
结局指标
主要结局
Time Until First Pain Medication Post-operatively
时间窗: 48 hrs
Time in minutes until first pain medication was take by participant post-operatively
次要结局
- Pain Score on Post Operative Day 1(1 day postoperative)
研究者
研究点 (1)
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