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临床试验/NCT06915974
NCT06915974招募中不适用

Comparison Between Interleukin 6 and Procalcitonin in Detecting Sepsis and Incidence of Mortality in Burn ICU Patients

Ain Shams University1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年1月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
70
试验地点
1
主要终点
Occurrence of sepsis and septic shock

研究概览

简要总结

The investigators will compare the efficacy of Interleukin-6 (IL-6) as a better indicator than procalcitonin in burn patients with sepsis or septic shock regarding success of treatment and early ICU discharge.

详细描述

Interleukin 6 and procalcitonin will be sampled for all patients on days 1, 3, 7, and 10.

Treatment plan will be initiated to all patients according to the burn ICU protocol.

According to the lab results, interleukin 6 and procalcitonin will guide the investigators to take decisions regarding clinical improvement and ICU stay.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
25 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with acute burn admitted to burn ICU within 24 hours from the burn incidence.
  • •patients with burn percentage of 25% to 50% of total body surface area
  • •patients with second to third degree burns
  • •ASA 1 and ASA 2 patients

排除标准

  • •Burn percentage more than 50% or less than 25% of total body surface area
  • •Having autoimmune diseases
  • •Cancer patients
  • •ASA 3 and ASA 4 patients

研究组 & 干预措施

Burn ICU patients

Experimental

Interleukin 6 and procalcitonin will be sampled for all patients on days 1, 3, 7, and 10. Treatment plan will be initiated to all patients according to the burn ICU protocol.

干预措施: Interleukin 6 (Diagnostic Test)

结局指标

主要结局

Occurrence of sepsis and septic shock

时间窗: From day 1 to day 10 in burn ICU

Prediction of occurrence of sepsis and septic shock

次要结局

  • Length of ICU stay(One month after ICU admission)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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