跳至主要内容
临床试验/NCT01838525
NCT01838525Unknown不适用

Alpha-1-acid Glycoprotein as a Biomarker of Developmental Diagnosing and Monitoring Effectiveness in Sepsis

Chinese PLA General Hospital1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2011年4月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
1
试验地点
1
主要终点
Patients Outcome

研究概览

简要总结

To assess the potential value of alpha-1-acid glycoprotein (AGP) for early diagnosis and prognosis of patients with sepsis, and then compared with C-reactive protein (CRP), procalcitonin (PCT), white blood cell (WBC) counts, Acute Physiology and Chronic Health Evaluation (APACHE) II score and Sequential Organ Failure Assessment (SOFA) score. 164 patients were enrolled in the study, including 25 cases with systemic inflammatory response syndrome (SIRS) and 139 cases with different levels of sepsis (46 moderate sepsis, 52 severe sepsis and 41 septic shock ). Serum levels of Alpha-1-acid Glycoprotein (AGP), C-reactive protein (CRP), and procalcitonin (PCT), and white blood cell (WBC) counts were measured on the day of admission to intensive care unit (ICU).

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • Male and female aged 18 years old and over;
  • Clinically suspected infection;
  • Fulfilled at least two criteria of systemic inflammatory response syndrome (a) core temperature higher than 38 °C or lower than 36 °C (b)respiratory rate above 20/min, or PCO2 below 32 mmHg (c) pulse rate above 90/min, and (d) white blood cell count greater than 12,000/μl or lower than < 4,000/μl or less than 10% of bands;

排除标准

  • less than 18 years old;
  • immunosuppression;
  • agranulocytosis (granulocyte counts <0.5× 109/L);
  • chronic myeloid leukemia (CML);
  • malignancy;
  • less than 24 hours of the length of ICU stay;
  • reluctant to participate in the study.

结局指标

主要结局

Patients Outcome

时间窗: 28 days

The survival time of patients more than 28 days is defined as survival. The survival time of patients less than 28 days is defined as death

次要结局

未报告次要终点

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Longxiang Su

Attending Doctor

Chinese PLA General Hospital

研究点 (1)

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