Comparison of Erector Spina Plan Block and Rhomboid Intercostal Block for Postoperative Pain Managment in Patients Undergoing Unilateral Breast Surgery
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 84
- 试验地点
- 2
- 主要终点
- Morphin Consumption
研究概览
简要总结
In this study, the investigators compared ultrasound-guided erector spinae plane (ESP) block and rhomboid intercostal block (RIB) on postoperative analgesic effect in unilateral breast surgery.
详细描述
After being informed about the study and potential risks, written consent was obtained from all patients.Patients who meet eligibility requirements will be randomized in a 1:1 ratio to erector spinae plane block and rhomboid intercostal block.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Diagnostic
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Patients who will undergo unilateral breast-conserving surgery (BCS) or modified radical mastectomy (MRM) with or without axillary lymph node dissection
- •Patients undergoing elective surgery
- •ASA (American Society of Anesthesiologists) physical status classification I-III
排除标准
- •Use of anticoagulants
- •Allergy to the medications to be used
- •Patients who use analgesic drugs due to a history of chronic pain
- •ASA (American Society of Anesthesiologists) physical status classification IV-V
- •Patients with psychiatric disorders
- •Presence of infection in the area where the block will be applied
- •Presence of deformity in the patient's spinal, paraspinal and area where the block will be applied
- •The patient does not accept the block application or cannot cooperate with the patient
研究组 & 干预措施
Erector Spinae Plane Block
Ultrasound(US)-guided erector spinae plan block(ESP) with 20 ml 0,25% bupivacaine at T4 vertebra level will performe preoperatively to all patients in the ESP group.
干预措施: Erector Spinae Plane Block (Other)
Rhomboid Intercostal Block
Ultrasound(US)-guided rhomboid intercostal block(RIB) with 20 ml 0,25% bupivacaine at T5-T6 vertebra level will performe preoperatively to all patients in the RIB group.
干预措施: Rhomboid Intercostal Block (Other)
结局指标
主要结局
Morphin Consumption
时间窗: during postoperative 24 hours
Patients in both groups will provide with intravenous patient-controlled analgesia device containing morphine for postoperative analgesia
次要结局
- Numerical Rating Scale(NRS)(during postoperative 24 hours)