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临床试验/NCT04313764
NCT04313764Unknown不适用

The Comparison of the Erector Spinae Plane Block and Wound Infiltration on Postoperative Opioid Consumption in Patients Undergoing Laparoscopic Colorectal Surgery

Ataturk University1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2020年6月18日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
48
试验地点
1
主要终点
Opioid Consumption

研究概览

简要总结

Colorectal cancer is a common and lethal disease. It still remains the third most common cause of cancer death in women and the second leading cause of death in men. Pain control is an important direction of postoperative management in malignancy surgery. Inadequate pain control increases cardiac and respiratory complications in these critical patients. Erector spinae plane (ESP) block is a recently described regional anesthesia technique that blocks the dorsal and ventral rami of the spinal nerves and the sympathetic nerve fibers. While the ESP block has been shown to provide effective postoperative analgesia after thoracic, and abdominal surgeries.

Our aim in this study was to investigate bilateral thoracic ESP block for providing successful postoperative pain management following colorectal surgery.

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 (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • American Society of Anesthesiologist's physiologic state I-II-III patients undergoing Colorectal surgery

排除标准

  • renal or hepatic insufficiency, chronic pain, patients with an allergic reaction to anesthesia and analgesia drugs to be used

研究组 & 干预措施

Group ESPB

Active Comparator

Ultrasound-guided erector spinae plane block with 20 ml %0.25 bupivacaine, per side

干预措施: Bupivacaine Hcl 0.25% ESP block (Drug)

Group Infiltration

Active Comparator

Wound infiltration with 20 ml %0.25 bupivacaine

干预措施: Bupivacaine Hcl 0.25% infiltration (Drug)

结局指标

主要结局

Opioid Consumption

时间窗: Postoperative first 24 hours

Opioid consumption postroperative period

次要结局

  • Visual Analog Pain Score(Postoperative first 24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ahmet Murat Yayik

Medical Doctor

Ataturk University

研究点 (1)

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