Efficacy of Ultrasound - Guided External Oblique Intercostal Plane Block for Patients Undergoing Upper Abdominal Surgeries: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 25
- 试验地点
- 1
- 主要终点
- Visual analogue pain scale .
研究概览
简要总结
Ithe study will evaluate the analgesic efficacy of external oblique intercostal block for patients undergoing upper abdominal surgeries
详细描述
Patients will be randomly divided into two equal groups using SPSS. Group A: will receive US-guided external oblique intercostal block after induction Group B: will receive postoperative morphine on patient request. Study design: prospective controlled randomized study.
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
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Selected patients will be more than 21 years old with ASA physical status I & II scheduled for upper abdominal surgeries
排除标准
- •Uncooperative patients.
- •Patients who have allergy to any of the used drugs.
- •Patients who are on opioids.
- •Known abuse of alcohol or medication.
- •Local infection at the site of injection or systemic infection.
- •Pregnancy
- •Patients with coagulation disorders or on anticoagulation therapy
研究组 & 干预措施
external oblique intercostal block
receive US-guided external oblique intercostal block after induction
干预措施: US-guided external oblique intercostal block (Other)
No block
receive postoperative morphine on patient request
结局指标
主要结局
Visual analogue pain scale .
时间窗: 24 hours
postoperative pain that evaluated by visual analogue pain scale(a scale from 0 to 10 where 0 is interpreted as no pain, 1-4 mild pain, 5-6 moderate pain, 7-10 severe pain)
次要结局
- total perioperative analgesics requirements(24 hours)
研究者
Amal Gouda Elsayed Safan
lecturer of anaethesia
Menoufia University