NCT06260137进行中（未招募）不适用
Comparison of the Effectiveness of the Combination of Rhomboid Intercostal and Sub-serratus Plan Block and Rhomboid Intercostal Block for Postoperative Analgesis in Video-assisted Thoracopic Surgery (VATS)
Uludag University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年7月10日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Postoperative analgesia
研究概览
简要总结
The goal of this clinical study is to compare the effectiveness of the Rhomboid Intercostal Block and Sub-Servitus plan block and the effectiveness of the Rhomboid intercostal block in patients with video-supported thoracoscopic surgery. The main question it aims to answer is:
Which of these two blocks more effectively reduces the patients' pain?
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Single (Participant)
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
- •Patients in American Society of Anesthesiologists (ASA) classes I, II and III for whom VATS is planned
排除标准
- •Known or suspected local anesthetic allergy
- •coagulopathy
- •injection site infection
- •history of thoracic surgery
- •serious neurological or psychiatric disorder
- •severe cardiovascular disease
- •liver failure
- •renal failure
结局指标
主要结局
Postoperative analgesia
时间窗: first 48 hours postoperatively
Patients' VAS scores and additional analgesic needs in the first 48 hours will be evaluated. VAS (visual pain scale) corresponds to a value between 0 and 10. A value of 0 means no pain, and a value of 10 is the most severe pain.
次要结局
未报告次要终点
研究者
Ferhat Ustuner
Research Assistant Doctor
Uludag University
研究点 (2)
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