NCT01075087已完成不适用
TAP) Block in Morbid Obese Patients Undergoing Laparoscopic Gastric Bypass Surgery: A Prospective,Randomized, Blinded Study
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 19
- 试验地点
- 1
- 主要终点
- Quality of Recovery 40 Score
研究概览
简要总结
The use of preoperative TAP block in laparoscopic bariatric surgery can improve the postoperative pain and quality of recovery in patients undergoing these procedures.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age: 18-65 years
- •BMI >35 Kg/m2
- •Surgery: laparoscopic gastric bypass surgery
- •ASA status: I, II and III
- •Fluent in English
排除标准
- •History of allergy to local anesthetics
- •Chronic opioid use
- •Pregnant patients
- •Patients who remained intubated after surgery
- •Drop-out criteria:
- •Patient or surgeon request Complications related to the procedure or conversion to open route Patient requiring mechanical ventilation after surgery
研究组 & 干预措施
Placebo
Placebo Comparator
(control group) will receive sterile normal saline in the block
干预措施: Placebo (Drug)
Active comparator
Active Comparator
(study group) will receive a bilateral TAP block using 20 cc of 0.5% ropivacaine on each side.
干预措施: (study group) will receive a bilateral TAP block using 20 cc of 0.5% ropivacaine on each side. (Drug)
结局指标
主要结局
Quality of Recovery 40 Score
时间窗: 24 hours post operatively
Quality of Recovery 40 Score at 24 hours postoperative.
次要结局
- 24 Hour Total Opioid Consumption.(24 hours)
研究者
Gildasio De Oliveira
Principal Investigator
Northwestern University
研究点 (1)
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