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临床试验/NCT07757984
NCT07757984尚未招募不适用

Regional Nerve Block for Upper Extremity Surgery in Patients With Sarcopenia

Chang Gung Memorial Hospital1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2026年9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
尚未招募
发起方
入组人数
150
试验地点
1
主要终点
time to first rescue analgesia

研究概览

简要总结

The goal of this observational study is to learn about the impact of sarcopenia (muscle loss) on the efficacy of regional nerve blocks and postoperative recovery in patients undergoing upper extremity surgery. The main questions it aims to answer are:

  1. Does sarcopenia affect the onset time and success rate of peripheral nerve blocks?
  2. How does sarcopenia influence postoperative pain control and opioid consumption compared to patients receiving pure general anesthesia?

Participants will undergo a preoperative muscle assessment, which includes a chair stand test and a brief ultrasound of the thigh muscle. Researchers will then observe and record their nerve block onset time (if applicable), postoperative pain scores, and recovery metrics during their hospital stay up to postoperative day 2.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age>=50 years old
  • •ASA I-III
  • •Receiving upper limb surgery under general anesthesia

排除标准

  • •Severe cognitive impairment or inability to cooperate with pain and motor assessment
  • •Pre-existing neuropathy of the musculocutaneous, median, radial or ulnar nerve
  • •(for nerve block group) Contraindications to regional nerve blockade

研究组 & 干预措施

General anesthesia alone

干预措施: sarcopenia (Other)

General anesthesia alone

干预措施: Non-sarcopenia (Other)

General anesthesia alone

干预措施: General Anesthesia (Procedure)

General anesthesia combine infraclavicular brachial plexus block, with sarcopenia

干预措施: sarcopenia (Other)

General anesthesia combine infraclavicular brachial plexus block, with sarcopenia

干预措施: General Anesthesia (Procedure)

General anesthesia combine infraclavicular brachial plexus block, with sarcopenia

干预措施: Nerve Block (Procedure)

General anesthesia combine infraclavicular brachial plexus block, without sarcopenia

干预措施: Non-sarcopenia (Other)

General anesthesia combine infraclavicular brachial plexus block, without sarcopenia

干预措施: General Anesthesia (Procedure)

General anesthesia combine infraclavicular brachial plexus block, without sarcopenia

干预措施: Nerve Block (Procedure)

结局指标

主要结局

time to first rescue analgesia

时间窗: From the completion of surgery up to Postoperative Day 2

次要结局

  • Postoperative NRSFrom the end of surgery up to 48 hours postoperatively.(From the end of surgery up to postoperative day 2)
  • Total opioid consumption(From the end of surgery up to postoperative day 2)
  • Nerve block onset(From the completion of local anesthetic injection up to 30 minutes)
  • Nerve block duration(From the successful onset of sensory block to the patient's first report of pain at the surgical site, assessed up to postoperatively day 2)
  • Intraoperative Mean Arterial Pressure (MAP) and Heart Rate (HR)(During surgery (From the induction of anesthesia to the end of surgery, an average of 2 hours))
  • Incidence of Local Anesthetic Systemic Toxicity (LAST)(From the initiation of nerve block up to 24 hours postoperatively)
  • Incidence of postoperative delirium(From the end of surgery up to postoperative day 2)
  • ICU stay(From ICU admission up to postoperative day 2)

研究者

发起方
Chang Gung Memorial Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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