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临床试验/ACTRN12613001366741
ACTRN12613001366741已完成未知

Randomised controlled trial of 24 hours intravenous (IV) antibiotic therapy followed by oral antibiotic therapy versus 72 hours or more IV antibiotic therapy for the successful resolution of acute erysipelas and cellulitis of the lower limb

Barwon Health0 个研究点目标入组 80 人开始时间: 2013年12月13日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
Barwon Health
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • 1.Acute cellulitis of lower limb with consistent clinical features, including; erythema, pain, and swelling with onset within 5 days with either fever on clinical examination or history consistent with fevers and/or chills, rigors, nausea within 5 days prior to presentation
  • 2.Age > 18 years
  • 3.Patient is planned for intravenous antibiotics via hospital admission or hospital-in-the-home treatment for cellulitis of the lower limb

排除标准

  • 1. Age <18 years
  • 2. Pregnant female
  • 3. Immunosuppression including any one of: active chemotherapy in the last 6 weeks, receipt of prednisolone >20mg/ day, or neutropaenia with neutrophil count <0.5 x 109/L or alternative conditions significantly affecting the immune system
  • 4. Alternative diagnosis, including but not limited to: venous eczema, Diabetic foot infection, Surgical site (wound) infection or other open wound
  • 5. Penetrating injury or bite
  • 6. Suspected complication such as abscess or necrotising infection
  • 7. Septic shock or other reasons for intensive care unit admission
  • 8. Oral antibiotics effective against cellulitis for > 48 hours or IV antibiotics effective against cellulitis for >24 hours. (including receipt of flucloxacillin, dicloxacillin, cephalexin, cephazolin, clindamycin and Vancomycin).
  • 9. Patient unwilling to participate or in the opinion of investigators will be unable to comply with the requirements of the study.

研究者

发起方
Barwon Health

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