Errector Spinae Plane Block for Postoperative Pain Management in Cardiac Surgery: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- change from baseline in pain the 10 point Visual Analog Scale (VAS) at hours 3,6,9,12,24,36,48.
研究概览
简要总结
The purpose of this study is to assess efficacy of erector spinae plane block (ESP) for postoperative pain management in cardiac surgery patients.
详细描述
After being informed about the study and potential risks, all patients giving written informed consent will be randomised (single blind) as block group(patients is performed esp block) and control group. All patients will be evaluate during 48 hours for postoperative pain.
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
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Must be ASA score I-III
- •Must be 18-75 years old
- •must undergo cardiac surgery
排除标准
- •emergency surgery,
- •bleeding diathesis,
- •presence of contraindications to LA agents used in this study,
- •use of chronic opioids,
- •psychiatric disorders.
- •prolonged extubation
- •presence of infection at the injection site.
- •cardiovascular conditions (EF<40, LMCA obstruction)
研究组 & 干预措施
esp block group
干预措施: erector spinae plane block (Procedure)
esp block group
干预措施: iv analgesia (Drug)
control group
干预措施: iv analgesia (Drug)
结局指标
主要结局
change from baseline in pain the 10 point Visual Analog Scale (VAS) at hours 3,6,9,12,24,36,48.
时间窗: baseline and hours 3-6-12-24-36-48
The VAS is validated instrument assessing average pain. Possible scores range from 0 (no pain) to 10 (worst possible pain) Change= (hours 3,6,9,12,24,48 score- baseline)
time to mobilize the patient
时间窗: Any time for 7 days
time to mobilize the patient is reported as when the patient is mobilized
次要结局
未报告次要终点
研究者
SINEM SARI
Assoc. Prof. Dr.
Aydin Adnan Menderes University