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临床试验/NCT04036812
NCT04036812已完成不适用

Ultrasound Guided Superficial Cervical Plexus Block for Analgesia After Craniotomy Via Suboccipital Retrosigmoid Approach: A Randomized Controlled Trial

Beijing Tiantan Hospital3 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2019年11月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
106
试验地点
3
主要终点
the cumulative consumption of sufentanil by the PCA

研究概览

简要总结

The incidence of postoperative pain after craniotomy is high. Severe postoperative pain can lead to a series of complications that are detrimental to the recovery of craniotomy patients. Compound local scalp nerve block is a good choice for analgesia after craniotomy. However, the scalp nerve block commonly cannot cover the area of suboccipital retrosigmoid approach craniotomy, leading to incomplete block. Superficial cervical plexus block (SCPB) is theoretically promising to solve the analgesia requirements of such surgical approach. At the same time, ultrasound guidance can not only accurately locate, ensure the effect of block and avoid accidental injury during puncture. The purpose of this study is to explore whether ultrasound-guided superficial cervical plexus block can safely and effectively reduce the requirement of analgesic drugs and pain after craniotomy via suboccipital retrosigmoid approach.

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
Quadruple (Participant, Care Provider, Investigator, 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

  • Elective suboccipital retrosigmoid approach approach craniotomy;
  • Age between 18 and 65 years;
  • American Society of Anesthesiologists (ASA) physical status I-III.

排除标准

  • The patients or legal clients refuse to provide informed consent;
  • Local infection;
  • Preoperative impairment of consciousness and cognitive function;
  • Uncontrolled hypertension;
  • Inability to communicate;
  • Allergies to experimental drugs;
  • History of drug abuse;
  • History of chronic headache;
  • Aphasia and hearing impairment;
  • Patients undergoing second craniotomy;
  • Body mass index < 18.5 kg/m2 or > 35.0 kg/m2;

结局指标

主要结局

the cumulative consumption of sufentanil by the PCA

时间窗: 24 hours after surgery

the cumulative consumption of sufentanil by the PCA 24 hours after surgery

次要结局

  • Use of analgesics by the PCA after operation(at 1, 2, 4, 48 hours after surgery.)
  • Pain severity score(at 1, 2, 4, 24, 48 hours after surgery)
  • Patient analgesic satisfaction(at 24 hours after surgery)
  • Anesthesia recovery quality score:(at 1 hour after surgery)

研究者

发起方
Beijing Tiantan Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yuming Peng

Associate professor

Beijing Tiantan Hospital

研究点 (3)

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