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临床试验/NCT03729427
NCT03729427撤回不适用

Erector Spinae Plane Block for Rib Cartilage Graft Reconstruction Surgery

Stanford University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
入组人数
50
试验地点
1
主要终点
Evaluating Pain Scores Using Faces, Legs, Activity, Cry, and Consolability (FLACC) Scale

研究概览

简要总结

The erector spinae plane block is a novel regional anesthetic technique that allows for analgesia of the thorax and abdomen with a peripheral nerve block. This study is being performed to assess the effectiveness of this technique in reducing post-operative pain scores and opiate requirements in pediatric and adult patients undergoing rib cartilage grafting surgeries.

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
2 Years 至 17 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Ages 2-17
  • •Able to consent (if greater than 7 years) and have parental consent
  • •Pediatric patients undergoing rib cartilage resection surgeries

排除标准

  • •Participants who do not consent or have parental consent
  • •Patients who are clinically unstable or requires urgent/emergent intervention

研究组 & 干预措施

Treatment Arm

Experimental

ESP Block

干预措施: Erector Spinae Plane Block (Procedure)

Control Arm

No Intervention

Standard of Care

结局指标

主要结局

Evaluating Pain Scores Using Faces, Legs, Activity, Cry, and Consolability (FLACC) Scale

时间窗: Duration of Study (Typically 4-5 days)

Scale will be used to asses pain initially prior to the procedure and postoperatively approximately every 6 hours.

Opiate Intake in Morphine Equivalents in Both Control and Treatment Group

时间窗: Duration of procedure and postoperative recovery (throughout study completion, typically 4-5 days)

Evaluating Pain Scores Using Wong-Baker FACES Pain Rating Scale

时间窗: Duration of Study (Typically 4-5 days)

Scale will be used to asses pain initially prior to the procedure and postoperatively approximately every 6 hours.

Evaluating Pain Scores Using 0-10 Numeric Pain Scale (0=No Pain, 10=Worst Pain)

时间窗: Duration of Study (Typically 4-5 days)

Scale will be used to asses pain initially prior to the procedure and postoperatively approximately every 6 hours.

次要结局

未报告次要终点

研究者

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

Chi-Ho Ban Tsui

Professor-Med Ctr Line

Stanford University

研究点 (1)

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