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临床试验/NCT04865211
NCT04865211Unknown2 期

Does a ThoracoLumbar Interfacial Plane (TLIP) Block With Liposomal Bupivacaine Provide Extended Post-operative Analgesia Following Spinal Surgery

The Cooper Health System1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年4月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
90
试验地点
1
主要终点
Reduction in postoperative pain

研究概览

简要总结

The investigators are looking to recruit patients into a study demonstrating the effectiveness of a superficial nerve block involving the thoracolumbar interfascial plane (TLIP) in reducing postoperative pain in those undergoing spinal surgery

详细描述

Patients undergoing spine surgery with or without fusion experience a great deal of pain especially in the first 3 days after surgery. Spine surgeons are looking for ways to reduce the pain that you experience. Anesthesiologists have introduced a procedure, called a "TLIP block" to provide pain relief. The block involves injecting local anesthetic (numbing pain medication) in the lower back around the site of the surgery. This block has been used by other surgeons for other types of surgeries in the past and has been shown to work.

To determine how effective the block is, the investigators are conducting this investigational study where pain severity in patients who receive one of 2 kinds of local anesthetic or placebo are compared

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients undergoing multilevel lumbar spine surgery, age 18-75

排除标准

  • Opioid use disorder, previous spine surgery, non english-speaking patients, patients with anticipated communication disorders, patients with coagulopathy, prisoners, children, pregnant women, single level hemilaminectomy with or without discectomy

研究组 & 干预措施

Liposomal Bupivicaine

Experimental

Administration of a combination of lioposomal bupivicane 20ml/266mg mixed with 20mL of 0.375% bupivicaine

干预措施: Liposomal bupivacaine (Drug)

Bupivicane

Active Comparator

Administration of 40 ml of 0.375% Bupivicaine with epinephrine 1:400,000

干预措施: Bupivacaine Injection (Drug)

Placebo

Placebo Comparator

Saline injection with 40mL preservative-free saline

干预措施: Placebo (Drug)

结局指标

主要结局

Reduction in postoperative pain

时间窗: 24-48 hours

Using Visual Analog Scales on a scale of 0-10, where 0 is no pain and 10 is the worst pain

Total postoperative opioid requirements

时间窗: 1-5 days

Using daily MME

次要结局

  • Length of Hospital Stay(1-5 days)
  • Time to Ambulation(1-5 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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