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The Relationship Between Vitamin D Levels, Inflammatory Parameters and Disease Severity of COVID-19 Infection

The Relationship Between Vitamin D Levels, Inflammatory Parameters and Disease Severity of COVID-19 Infection: A Retrospective Study

Vitamin D deficiency increases the susceptibility to respiratory virus infections and the severity of infections. Inflammation plays a key role in pathogenesis in COVID19 while identifying clinical course and prognosis COVID19.The aim of this study was to determine the relationship between 25OH vitamin D levels, inflammatory laboratory parameters of neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR), C-reactive protein (CRP) levels and disease severity of COVID19 infection.

研究概览

详细说明

In this retrospective study 300 patients diagnosed with COVID19 were included. According to clinical classification of cases with COVID19 the patients were divided into three groups; mild (Group1), moderate (Group2) and severe/critical (Group3). The 25OH vitamin D values below 20 ng/ml were defined as deficiency, 21-29 ng/ml were defined as insufficiency, and 30 ng/ml and above were defined as normal. Patients' age, gender, comorbid diseases and laboratory values were recorded

研究类型

观察性的

注册 (实际的)

300

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Istanbul、火鸡、34752
        • Gulcan Ozturk

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

16年 至 97年 (孩子、成人、年长者)

接受健康志愿者

不适用

有资格学习的性别

全部

取样方法

非概率样本

研究人群

COVID19 infection positive patients whose polymerase chain reaction (PCR) test positive patients and whose 25-OH vitamin D levels were measured in the last 6 months

描述

Inclusion Criteria:

  • The study included 300 polymerase chain reaction (PCR) test positive patients and whose 25-OH vitamin D levels were measured in the last 6 months

Exclusion Criteria:

  • Patients with COVID-19 whose 25-OH vitamin D levels were not measured in the last 6 months before the COVID-19 diagnosis were excluded from the study

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Experimental: Mild Clinical Group
patients showing mild clinical symptoms without pneumonia.
Laboratory measurement of patient's inflammatory status in unit of % and mg/dl
Laboratory measurement of patient's 25 OH vitamin D level in unit of ng/dl
Experimental: Moderate Clinical Group
patients with fever, other respiratory symptoms, and pneumonia findings based on radiological imaging
Laboratory measurement of patient's inflammatory status in unit of % and mg/dl
Laboratory measurement of patient's 25 OH vitamin D level in unit of ng/dl
Experimental: severe/critical clinical group
severe one of these as follows; patients with hypoxia (≤93% oxygen saturation), respiratory distress (RR >30 times per minute), partial pressure of arterial blood oxygen (PaO 2 )/the fraction of inspired oxygen (FiO 2 ) ≤ 300 mmHg, patients whose chest imaging shows that lung damage develops significantly within 24 to 48 hours, or critical one of these as follows; respiratory failure requiring mechanical ventilation, signs of septic shock with multiple organ failure requiring intensive care unit admission.
Laboratory measurement of patient's inflammatory status in unit of % and mg/dl
Laboratory measurement of patient's 25 OH vitamin D level in unit of ng/dl

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
25-OH vitamin D
大体时间:1 day
laboratory measurement in unit of ng/ml
1 day
White blood cell count
大体时间:1 day
laboratory measurement in unit of x103/uL
1 day
neutrophil count
大体时间:1 day
laboratory measurement in unit of x103/uL
1 day
neutrophil ratio
大体时间:1 day
laboratory measurement in unit of %
1 day
lymphocyte count
大体时间:1 day
x103/uL
1 day
lymphocyte ratio
大体时间:1 day
laboratory measurement in unit of %
1 day
platelet count
大体时间:1 day
laboratory measurement in unit of x103/uL
1 day
hemoglobin count
大体时间:1 day
laboratory measurement in unit of g/dl
1 day
C-reactive protein levels
大体时间:1 day
laboratory measurement in unit of mg/dL
1 day
neutrophil to lymphocyte ratio
大体时间:1 day
laboratory measurement in unit of %
1 day
platelet to lymphocyte ratio
大体时间:1 day
laboratory measurement in unit of %
1 day

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2020年7月1日

初级完成 (实际的)

2020年8月1日

研究完成 (实际的)

2020年8月1日

研究注册日期

首次提交

2021年6月6日

首先提交符合 QC 标准的

2021年6月28日

首次发布 (实际的)

2021年6月30日

研究记录更新

最后更新发布 (实际的)

2021年6月30日

上次提交的符合 QC 标准的更新

2021年6月28日

最后验证

2021年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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