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临床试验/NCT03682354
NCT03682354已完成不适用

Erector Spinae Plane Block Versus Intercostal Nerve Block Combined With Patient-controlled Intravenous Analgesia in Video-assisted Thoracic Surgery

Peking University Third Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2018年9月27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
状态
已完成
入组人数
70
试验地点
1
主要终点
Pain score (NRS)

研究概览

简要总结

A randomized prospective trial to test the non-inferiority of erector spinae plane block (ESPB) in comparison with intercostal nerve block combined with patient-controlled intravenous analgesia in Thoracoscopic lung surgery

详细描述

For patients undergoing thoracic surgery, postoperative pain greatly limited their recovery.Multimodal analgesia have shown good efficacy but without reaching full pain relief.

The primary goal of this study is to observe the effect of ultrasound-guided erector spinae plane block in comparison with intercostal nerve block combined with patient-controlled intravenous analgesia in video assisted thoracic lung 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
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients to receive video assisted thoracoscopic lobectomy or bullectomy .

排除标准

  • Patient refusal
  • Heavy skin eruption and infection at site of injection.
  • Coagulopathy.
  • Allergy to local anesthetics.
  • Taking analgesics.

研究组 & 干预措施

Intercostal Nerve Block with PCIA

Active Comparator

Intercostal Nerve Block with patient-controlled intravenous analgesia

干预措施: Intercostal Nerve Block with PCIA (Drug)

Erector Spinae Plane Block (ESPB)

Experimental

Continuous Erector Spinae Plane Block

干预措施: Erector Spinae Plane Block (ESPB) (Drug)

结局指标

主要结局

Pain score (NRS)

时间窗: 4 hours from the end of procedure

Numeric Rating Scale is an 11-point scale used by doctors to evaluate patients' pain, where 0 is no pain and 10 the worst imaginable pain. For postoperative patients, an higher score shows inadequate analgesia and worse outcome.

次要结局

  • Pain score (NRS)(8, 24,48 hours from the end of procedure)
  • Incidence of side effects and complication during study(During operation,4, 8, 24,48 hours from the end of procedure)
  • Analgesics consumption(During operation,4, 8, 24,48 hours from the end of procedure)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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