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临床试验/NCT02443272
NCT02443272已完成不适用

A Randomized Comparison Study of Minimally Invasive Loop Drainage Versus Standard Incision and Drainage for Skin Abscesses in Children

Seton Healthcare Family1 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2014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
已完成
入组人数
81
试验地点
1
主要终点
Treatment failure

研究概览

简要总结

The purpose of this study is to compare abscess drainage utilizing the vessel loop technique in children to the standard incision and drainage technique with the endpoint to determine if rates of treatment failure are non-inferior.

详细描述

BACKGROUND INFORMATION:

Infections of skin and soft tissue remain one of the more common chief complaints in the pediatric emergency department. With methicillin-resistant Staphylococcus aureus being a prevalent pathogen, abscess development is not uncommon. The emergency department remains the common setting for required therapeutic intervention. However, active investigation exists in regard to the ideal intervention for children and adults.

Incision and drainage of cutaneous abscess has remained the standard of care for years. However this standard has been adopted without robust supportive evidence. Recently, various studies have questioned the benefit of various aspects of treatment, including antibiotics, incision size, and necessity for packing. Other studies have even suggested a less-invasive approach. Some of these have utilized a vessel loop and have demonstrated a reduced need for home-health visits, reduced inpatient length of stay, good patient tolerance, and no increase in failure rates. These studies are, however, retrospective in design with execution primarily by the surgical team.

STUDY DESCRIPTION:

Upon obtaining written informed consent/assent by the study team member, subjects will be randomized using a computerized randomization procedure and opaque envelopes. Initially, thorough history and physical exam will be performed. A data sheet will be completed detailing patient characteristics (eg. age, gender, ethnicity, prior treatment) and wound characteristics (eg. greatest diameter of both erythema and induration, presence of spontaneous drainage, location). Pain control/procedural sedation will be selected at the discretion of the treating physician, consistent with current local practice (eg. topical lidocaine, intranasal fentanyl and/or midazolam, oral acetaminophen/hydrocodone or ibuprofen, intravenous ketamine, morphine, or fentanyl). Pain will be assessed prior to physical exam and again shortly after the procedure via the validated FACES-Revised Pain Scale. The patient will provide this assessment if 5 years or older. Otherwise, the parent will provide the degree of pain perceived for their child. The difference between these two pain assessments will be evaluated as an endpoint. Physicians will report on their satisfaction with the procedure using a 5-point Likert scale.

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
29 Days 至 17 Years(Child)
性别
All
接受健康志愿者
是

入选标准

  • •Physical findings suggestive of skin abscess warranting incision and drainage (determined by treating physician)

排除标准

  • •Abscess not suitable for drainage in the ED (eg. <1 cm induration, >15 cm induration)
  • •Immunocompromised status (eg. diabetic patient or taking immunosuppressive medication)
  • •Need for hospitalization following drainage
  • •Abscess located above the clavicles or significantly involving genitals/pilonidal region
  • •Previous instrumentation to the abscess
  • •Primary language not English or Spanish
  • •High probability of loss to follow up (parent does not commit to both mandatory follow up appointments)

研究组 & 干预措施

Control Arm

Active Comparator

Receive standard incision and drainage

干预措施: Incision and Drainage (Procedure)

Intervention Arm

Experimental

Receive minimal invasive loop drainage using the Vesi-loop device

干预措施: Vessel Loop Drainage (Procedure)

结局指标

主要结局

Treatment failure

时间窗: 14 days

Requiring reinstrumentation of abscess, or hospital admission for IV antibiotics

次要结局

  • Physician satisfaction with procedure(1 Day)
  • Level of anxiety with wound care at home(14 Days)
  • Parental satisfaction with procedure(1 Day)
  • Cosmetic success(14 Days)
  • Pain reduction with drainage procedure(1 Day)
  • Parental satisfaction with scar(90 Days)
  • Frequency of post-drainage visits to a physician(14 Days)
  • Level of simplicity with wound care at home(14 Days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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