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临床试验/NCT06271707
NCT06271707招募中4 期

Left Sided Stellate Ganglion Blocks Impact on the Rate of Post-operative Atrial Fibrillation in Patients Undergoing Thoracic Surgery: A Pilot Study

University of Minnesota1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2025年5月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
入组人数
48
试验地点
1
主要终点
an ultrasound guided left stellate ganglion block with 5 mL of saline.

研究概览

简要总结

The purpose of this study is to determine if the addition of an ultrasound guided left sided stellate ganglion block with bupivacaine in patients undergoing esophagectomy, pneumonectomy, or lobectomy will result in lower rates of postoperative atrial fibrillation as compared to standard of care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

This is a double blind randomized prospective controlled trial. Randomization will be 1:1.

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing esophagectomy, pneumonectomy, or lobectomy aged 18-85.

排除标准

  • Patients who have an exclusion to regional anesthesia.
  • Patients who have exclusion to stellate blockade.
  • Patients who are pregnant assessed via self-report or pregnancy test if they have taken one

研究组 & 干预措施

Group 1

Experimental

ultrasound with bupivacaine

干预措施: 0.5% bupivacaine (Drug)

Group 2

Sham Comparator

Ultrasound with saline

干预措施: Saline (Other)

结局指标

主要结局

an ultrasound guided left stellate ganglion block with 5 mL of saline.

时间窗: 168 hours after surgery

Incidence of Atrial fibrillation in the first 168 hours after surgery.

Atrial fibrillation; Other arrhythmias; Adverse events.

时间窗: 168 hours after surgery

Atrial fibrillation in first 24, 48, 72, 96, 120, and 144 hours; Other arrhythmias in first 24, 48, 72, 96, 120, 144 and 168 hours; Adverse events.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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