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临床试验/NCT03173326
NCT03173326终止不适用

Randomized Controlled Trial Evaluating Patient Satisfaction and Postoperative Analgesia Between Subarachnoid Block With 2-chloroprocaine Versus General Anesthesia for Knee Arthroscopy

Vanderbilt University Medical Center2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2017年6月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
2
主要终点
Opioid utilization

研究概览

简要总结

The study evaluates the efficacy of two different anesthetic techniques in patients undergoing unilateral knee arthroscopy. Participants will be randomized to receive either subarachnoid block with 2-chloroprocaine or general anesthesia plus intravenous fentanyl.

详细描述

The study evaluates the efficacy of two different anesthetic techniques in patients undergoing unilateral knee arthroscopy. Participants will be randomized to receive either subarachnoid block with 2-chloroprocaine or general anesthesia plus intravenous fentanyl. The study evaluates pain scores, opioid utilization and patient satisfaction.

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
30 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with ASA physical status classification of I, II, or III
  • Patients without a current diagnosis of chronic pain or chronic opioid use for > 1-month prior to knee arthroscopy
  • Patients who are scheduled to undergo unilateral knee arthroscopy
  • Patients do not have a contraindication to receiving regional anesthesia

排除标准

  • Preexisting sensory or motor deficit in operative extremity
  • Patients with a contraindication to general anesthesia
  • Patient undergoing meniscal or ligamentous repair

研究组 & 干预措施

Subarachnoid block

Experimental

干预措施: Subarachnoid block (Procedure)

General anesthesia

Active Comparator

干预措施: General anesthesia (Procedure)

结局指标

主要结局

Opioid utilization

时间窗: Three months postoperatively

Opioid utilization based on average number of pain pills taken per day

Pain score

时间窗: Three months postoperatively

Pain score measured with a patient reported 11 point Numeric Rating Pain Scale with 0 indicating no pain and 10 indicating worst pain imaginable.

次要结局

  • Patient satisfaction with anesthetic(24 hours after PACU discharge)

研究者

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

Jenna Walters

Assistant Professor

Vanderbilt University Medical Center

研究点 (2)

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