NCT03852862已完成4 期
Double Regional Anesthesia in Video Assisted Thoracoscopy
University Hospital, Rouen1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2019年5月8日最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 112
- 试验地点
- 1
- 主要终点
- Number of opioids drug administrated
研究概览
简要总结
Monocentric, randomized, controlled, single-blind study who's aim is to demonstrate the efficacy of the association of paravertebral block and serratus plane block with paravertebral block alone
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient aged 18 to 75 years;
- •Programmed for unilateral videothoracoscopy for anatomical resection (segmentectomy, lobectomy);
- •Subject affiliated to a social security scheme;
- •Subject having signed an informed consent
排除标准
- •Chronic treatment with opiates;
- •Contraindication to administration of morphine;
- •Allergy to local anesthetics or contraindications to the use of ropivacaine;
- •Contraindication to the realization of paravertebral blocks and serratus;
- •Pregnancy, breastfeeding;
- •Severe obesity (BMI > 40 kg/m²);
- •Renal impairment (GFR < 30 mL/min) or known severe hepatic impairment;
- •Difficulties of comprehension preventing the collection of consent and the realization of the study;
研究组 & 干预措施
Serratus plane block with paravertebral block
Experimental
Association of Serratus plane block and paravertebral block for anesthesia
干预措施: Serratus plane block and paravertebral block (Drug)
paravertebral block alone
Active Comparator
Paravertebral block for anesthesia
干预措施: paravertebral block (Drug)
结局指标
主要结局
Number of opioids drug administrated
时间窗: 24 hours postoperatively
次要结局
- Length of stay in recovery room(24 hours postoperatively)
- Total duration of hospitalization(during the 28 days postoperatively)
研究者
研究点 (1)
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