Erector Spinae Plane Block Versus Oblique Subcostal Transverses Abdominis Plane Block for Controlling Postoperative Pain After Umbilical Hernia Repair
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 52
- 试验地点
- 2
- 主要终点
- Postoperative analgesic requirements
研究概览
简要总结
Comparing the impact of bilateral erector spinae plane block and transverse abdominis plane block on improving quality of pain management after umbilical hernia repair.
详细描述
Postoperative pain is an important problem after umbilical hernia repair which has negative effects on patient's hemodynamics and cause delayed ambulation resulting in prolonged duration of hospital stay and poor patient satisfaction.
Multiple analgesic strategies have been proposed including Non steroidal anti-inflammatory drugs (NSAIDs), opioids, epidural analgesia. Each of them has its limitations.
Ultra¬sound guided regional anesthesia techniques for abdominal wall can be effective components of multimodal postoperative analgesia with limited side-effects Erector spinae plane (ESP) block is a promising para-spinal bock that can achieve both visceral and somatic abdominal analgesia if the injection was performed at a lower thoracic level. Transverse abdominis plane (TAP) block which is considered a peripheral nerve block that is aimed at anesthetizing nerves supplying the anterior abdominal wall.
We will compare between erector spinae plane block and transverse abdominis plane block for controlling postoperative pain after umbilical hernia repair.
Patients will be allocated randomly into two equal groups by a computer-generated randomization table Group (E) (n=26): Patients will receive erector spinae plane (ESP) block after completion of surgery.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 21 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Patients scheduled for elective umbilical hernia repair.
- •Patient acceptance.
- •Patient's age 21 - 60 years.
- •Patients with American Society of Anesthesiologists (ASA) physical status I, II.
- •BMI 25 - 30 kg m-2.
排除标准
- •Uncooperative patients and patients with psychological problems.
- •Patients with liver or renal impairment.
- •Patients with contraindication to regional anesthesia.
- •Patients with history of allergy to drug used in the study.
- •Patients with chronic pain.
结局指标
主要结局
Postoperative analgesic requirements
时间窗: 24 hours postoperative
measuring the total doses of analgesic required to relieve the pain
次要结局
- Postoperative heart rate changes(24 hours postoperative)
- Postoperative pain severity using Numeric Rating Scale(24 hours postoperative)
- Postoperative blood pressure changes(24 hours postoperative)
- Duration of postoperative hospital stay(24 hours postoperative)
- Postoperative pain severity using Visual Analogue scale(24 hours postoperative)
- Incidence of postoperative side effects(24 hours postoperative)
- Postoperative pain severity using Verbal Rating Scale(24 hours postoperative)
研究者
Michael Adel Shaker
lecturer of anaesthesia and intensive care
Zagazig University