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Effect of Preoperative Ultrasound-Guided Stellate Ganglion Block on Postoperative Delirium in Older Adults Undergoing Elective Peripheral Endovascular Intervention

2026年9月26日 更新者:Loay Gamal、Assiut University

Effect of Preoperative Ultrasound-Guided Stellate Ganglion Block on Postoperative Delirium in Older Adults Undergoing Elective Peripheral Endovascular Interventions: A Randomized Controlled Trial.

This randomized controlled trial will evaluate whether preoperative ultrasound-guided stellate ganglion block reduces the incidence of postoperative delirium in adults aged 60 years or older undergoing elective peripheral endovascular interventions. Participants will be randomly allocated in a 1:1 ratio to receive either a right-sided ultrasound-guided stellate ganglion block at the C6 level with 5 mL of 0.375% ropivacaine or a control group. Postoperative delirium will be assessed twice daily during the first 3 postoperative days using the 3-Minute Diagnostic Interview for Confusion Assessment Method-defined Delirium (3D-CAM).

研究概览

地位

尚未招聘

详细说明

Postoperative delirium is a frequent complication among older adults undergoing surgery and vascular interventions. This study will investigate whether preoperative ultrasound-guided stellate ganglion block can reduce postoperative delirium through modulation of sympathetic activity and potentially inflammatory responses.

Eligible participants aged 60 years or older undergoing elective peripheral endovascular interventions will be randomly allocated in a 1:1 ratio to an active stellate ganglion block group or control group. The active intervention will consist of a right-sided ultrasound-guided stellate ganglion block performed at the C6 level approximately 30 minutes before surgery, using a 22-gauge needle and 5 mL of 0.375% ropivacaine. The control group will receive standard perioperative care and regional anesthesia according to the study protocol, but no stellate ganglion block or sham procedure will be performed

All participants will receive standardized anesthesia consisting of ultrasound-guided combined femoral and sciatic nerve blocks with bupivacaine, supplemented by dexmedetomidine sedation.

The primary outcome will be cumulative incidence of postoperative delirium from postoperative day 1 through postoperative day 3, assessed twice daily using the 3D-CAM. Secondary outcomes will include delirium severity, delirium duration, postoperative pain, opioid consumption, and safety/adverse events.

研究类型

介入性

注册 (估计的)

168

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

65年 及以上 (年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age ≥65 years.
  2. Scheduled for elective peripheral endovascular interventions.
  3. American Society of Anesthesiologists (ASA) physical status I-III.
  4. Ability to provide written informed consent or consent through a legal representative

Exclusion Criteria:

  1. Preexisting cognitive impairment (Montreal Cognitive Assessment score below the education-adjusted cutoff) or diagnosed dementia.
  2. Severe visual or hearing impairment or language barrier precluding reliable delirium assessment.
  3. Major psychiatric disorders, including schizophrenia or bipolar disorder.
  4. Contraindications to stellate ganglion block, including local infection at the puncture site, known allergy to local anesthetics, or severe coagulopathy.
  5. Severe systemic disease, including Child-Pugh C liver cirrhosis, end-stage renal disease (eGFR <30 mL/min/1.73 m² or dialysis), or NYHA class III-IV heart failure.
  6. Emergency surgery.
  7. History of substance abuse

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Ultrasound-Guided Stellate Ganglion Block

Participants will receive a right-sided ultrasound-guided stellate ganglion block at the C6 level approximately 30 minutes before surgery. Under sterile conditions and real-time ultrasound guidance, a 22-gauge needle will be advanced to the prevertebral fascia. After negative aspiration, 5 mL of 0.375% ropivacaine will be injected. Successful sympathetic blockade will be assessed by development of Horner's syndrome and/or a relative increase in ipsilateral skin temperature of ≥1.5°C within 15 minutes after injection

5 mL of 0.375% ropivacaine administered during ultrasound-guided right stellate ganglion block at the C6 level approximately 30 minutes before surgery.

无干预:control group

the participants will receive standard perioperative care and regional anesthesia according to the study protocol, but no stellate ganglion block or sham procedure will be performed

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Cumulative incidence of postoperative delirium
大体时间:postoperative 24 hours , 48 hours , 72 hours.

.Postoperative delirium will be assessed twice daily during the first 3 postoperative days using the 3-Minute Diagnostic Interview for Confusion Assessment Method-defined Delirium (3D-CAM). A participant will be considered to have developed postoperative delirium if at least one postoperative delirium assessment is positive during the first 3 postoperative days.

postoperative 24 hours , 48 hours , 72 hours.

次要结果测量

结果测量
措施说明
大体时间
Delirium severity
大体时间:postoperative 24 hours , 48 hours , 72 hours , among participants diagnosed with postoperative delirium

the severity of delirium will be graded using Memorial Delirium Assessment Scale (MDAS)

postoperative 24 hours , 48 hours , 72 hours , among participants diagnosed with postoperative delirium
Duration of postoperative delirium
大体时间:postoperative 24 hours , 48 hours , 72 hours.

Number of postoperative days with a positive 3D-CAM assessment

postoperative 24 hours , 48 hours , 72 hours.
Postoperative pain intensity
大体时间:Immediate postoperative period 2 hours 6 hours 12 hours 24 hours

Postoperative pain intensity will be assessed by Numerical Rating Scale (NRS)

Immediate postoperative period 2 hours 6 hours 12 hours 24 hours
Total postoperative opioid consumption
大体时间:postoperative 24 hours , 48 hours , 72 hours.

by Morphine milligram equivalents (MME)

postoperative 24 hours , 48 hours , 72 hours.
Safety and adverse events
大体时间:postoperative 24 hours , 48 hours , 72 hours.
postoperative 24 hours , 48 hours , 72 hours.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

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一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月1日

初级完成 (估计的)

2027年10月1日

研究完成 (估计的)

2028年5月1日

研究注册日期

首次提交

2026年9月19日

首先提交符合 QC 标准的

2026年9月26日

首次发布 (实际的)

2026年9月29日

研究记录更新

最后更新发布 (实际的)

2026年9月29日

上次提交的符合 QC 标准的更新

2026年9月26日

最后验证

2026年9月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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