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临床试验/NCT05642026
NCT05642026招募中4 期

The Efficacy of Continuous Intercostal Nerve Blocks in the Treatment of Patients With Multiple Rib Fractures

Zachary Warriner1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2025年9月23日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
180
试验地点
1
主要终点
Length of hospital stay

研究概览

简要总结

This is a prospective, randomized, non-blinded study comparing CINB plus medical therapy versus standard medical care (non-steroidals and opioids intravenous/oral inpatient and oral outpatient) alone for patients with multiple rib fractures. The objective of this study is to analyze the effect of continuous intercostal nerve block (CINB) in the treatment of patients admitted to the adult trauma service with rib fractures. The effectiveness of CINB as adjunctive treatment will be compared to standard medical therapy involving nonsteroidal and intravenous/oral opioid medications.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects will be at least 18 years old
  • Subjects will have 2 or more identified rib fractures
  • Subjects will be willing to provide informed consent for procedure
  • Subjects will be identified as appropriate for initiation of continuous nerve block therapy for treatment of rib fracture associated pain.

排除标准

  • Documented allergy to study medication
  • Epidural catheter use
  • Prisoners
  • Refusal of CINB therapy

研究组 & 干预措施

continuous intercostal nerve block (CINB)

Experimental

patients admitted to the adult trauma service with rib fractures who are receiving CINB

干预措施: Ropivacaine (Drug)

continuous intercostal nerve block (CINB)

Experimental

patients admitted to the adult trauma service with rib fractures who are receiving CINB

干预措施: Non steroidal anti-inflammatory drug and opioids (Drug)

standard medical care

Active Comparator

patients admitted to the adult trauma service with rib fractures who are receiving standard medical care

干预措施: Non steroidal anti-inflammatory drug and opioids (Drug)

结局指标

主要结局

Length of hospital stay

时间窗: 7 days

time from randomization until the time of discharge

次要结局

  • Patient reported quality of life(7 days)
  • Patient daily pain scores(7 days)
  • Modified Morphine Equivalent (MME) differences(7 days)
  • spirometry values(7 days)
  • hospital-free days(30 days)
  • mean respiratory rates(7 days)

研究者

发起方
Zachary Warriner
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Zachary Warriner

Assistant Professor

University of Kentucky

研究点 (1)

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