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临床试验/NCT05831774
NCT05831774进行中(未招募)4 期

Intraosseous vs. Intravenous Vancomycin Administration in Total Shoulder Arthroplasty: Changing the Paradigm

The Methodist Hospital Research Institute1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2023年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
进行中(未招募)
入组人数
33
试验地点
1
主要终点
Systemic Levels of Vancomycin

研究概览

简要总结

The purpose of this study is to compare two different antibiotic regimens and techniques during total shoulder arthroplasty.

Primary Objective: Comparable levels of vancomycin will be found in bone, soft tissue, and systemic samples between patient groups.

Secondary Objective: Compare 30 day and 90 day post-operative complication rates (infection) between the control (standard IV administration of vancomycin) vs the interventional group (intraosseous administration of vancomycin). The investigators hypothesize that there will be no difference in complication (infection) rates between groups.

详细描述

This study is a prospective, randomized, single-blinded, controlled trial. 20 patients in each treatment arm: 20 patients will be given IV vancomycin, 20 patients will be given IO vancomycin. This sample size is based on previous studies examining vancomycin concentration in tourniquetless primary total knee arthroplasty between IO vs IV [12,13].

Once the participant has been enrolled, they will be randomized into either the control group or the experimental group by an excel-based software program prior to their procedure.

Control - Standard IV administration of vancomycin

1) Patients will receive the Houston Methodist Hospital orthopedic surgeon's standard of care pre-operative antibiotic regimen for primary total shoulder arthroplasty patients. This includes IV abx (typically ancef or cefepime and vancomycin) will be started in the pre-operative period approximately 1 hour prior to incision (vancomycin dose weight-based at approximately 15mg/kg [6,7] generally 1000-1750mg in 500mL NS).

Intervention - Intraosseous (IO) administration of vancomycin

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
Double (Participant, Investigator)

盲法说明

Double blinded study

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

  • 未提供

排除标准

  • Previous shoulder surgery
  • BMI above 35
  • Contraindication to receiving vancomycin, cefepime, ancef, or other standard of care pre-operative antibiotic (allergy, medical issue, etc).
  • Inability to administer the IO infusion
  • Refusal to participate
  • Immunocompromised or immunosuppressed patients (HIV, Hep C, ESRD, dialysis, transplant, chemo/radiation treatment in last 6 months, medications)

研究组 & 干预措施

Control - Standard IV administration of vancomycin

Placebo Comparator

Patients will receive the Houston Methodist Hospital orthopedic surgeon's standard of care pre-operative antibiotic regimen for primary total shoulder arthroplasty patients. This includes IV abx (typically ancef or cefepime and vancomycin) will be started in the pre-operative period approximately 1 hour prior to incision (vancomycin dose weight-based at approximately 15mg/kg [6,7] generally 1000-1750mg in 500mL NS).

干预措施: Control - Standard IV administration of vancomycin (Drug)

Intervention - Intraosseous (IO) administration of vancomycin

Experimental
  • IV antibiotics (per physician's standard of care): Typically ancef or cefepime is started in pre-op within 1 hour of incision
  • IO vancomycin is administered in the OR after sterile prep and draping has occurred (500mg in 100-150mL NS).
  • Injection will take place into the proximal humerus

干预措施: Intervention - Intraosseous (IO) administration of vancomycin (Drug)

结局指标

主要结局

Systemic Levels of Vancomycin

时间窗: 24 hours

Comparable levels of vancomycin will be found in systemic samples between patient groups.

Vancomycin Levels in the Initial Deltoid

时间窗: 24 hours

Comparable levels of vancomycin will be found in the initial deltoid samples between patient groups.

Vancomycin Levels in the Humeral Head

时间窗: 24 hours

Comparable levels of vancomycin will be found in humeral head samples between patient groups.

Levels of Vancomycin in Synovium

时间窗: 24 hours

Comparable levels of vancomycin will be found in synovium samples between patient groups.

Levels of Vancomycin in Labrum

时间窗: 24 hours

Comparable levels of vancomycin will be found in labrum samples between patient groups.

Levels of Vancomycin in Glenoid Reaming

时间窗: 24 hours

Comparable levels of vancomycin will be found in glenoid reaming samples between patient groups.

Levels of Vancomycin in Bicep Tendon

时间窗: 24 hours

Comparable levels of vancomycin will be found in bicep tendon samples between patient groups.

Levels of Vancomycin in End Deltoid

时间窗: 24 hours

Comparable levels of vancomycin will be found in end deltoid samples between patient groups.

Vancomycin Levels in Bicep Tendon

时间窗: 24 hours

Comparable levels of vancomycin will be found in bicep tendon samples between patient groups.

次要结局

  • Post-operative Complication (Infection) Rates(30 days, 90 days)

研究者

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

Patrick McCulloch,MD

Principal Investigator

The Methodist Hospital Research Institute

研究点 (1)

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