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临床试验/NCT04738760
NCT04738760已完成不适用

Clinical Outcomes of High Dose Vitamin D Versus Standard Dose in COVID-19 Egyptian Patients

Ain Shams University1 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2020年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
116
试验地点
1
主要终点
In-hospital mortality

研究概览

简要总结

Vitamin D is a secosteroid hormone which may have beneficial role in reducing COVID-19 adverse outcomes by first regulating the renin angiotensin system (RAS). Recent studies on animal in which acute respiratory distress syndrome (ARDS) was induced, showed that vitamin D lead to pulmonary permeability reduction by modulating RAS activity as well as the expression of the angiotensin-2 converting enzyme (ACE2). During COVID-19, downregulation of ACE2 leads to cytokine storm in the host, causing ARDS. In contrast, an experimental study conducted on mice in which ARDS was induced chemically, revealed that vitamin D admiration contributed to mRNA and ACE2 proteins levels improvement, ADRS milder symptoms as well as less lung damage.

Additionally, vitamin D had shown antiviral effects on several previous studies, that though to be exerted either by antimicrobial peptides induction which subsequently had direct antiviral action or through immunomodulatory and anti-inflammatory effects.

In addition, vitamin D stabilizes physical barriers which prevent viruses from reaching tissues susceptible to infection. Finally, previous studies demonstrated that hypovitaminosis D is accompanied by various comorbidities including diabetes mellitus, hypertension, chronic cardiovascular and respiratory diseases, and cancers, all medical conditions that are considered risk factors of COVID-19 infection deterioration and even high mortality rate.

The objective of this study is to evaluate whether supplementation with high-dose vitamin D improves the prognosis of patients diagnosed with COVID-19 compared to a standard dose of vitamin D.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 to 65 years.
  • COVID-19 hospitalized patients with pneumonia confirmed by chest X-ray or CT scan.
  • RT-PCR Confirmed infection with COVID-19 or strongly suspected infection with pending confirmation studies.
  • Presence of acute respiratory distress syndrome (ARDS).
  • Having either peripheral capillary oxygen saturation (SpO2) ≤ 94% ambient air, or a partial oxygen pressure (PaO2) to fraction of inspired oxygen (FiO2) ratio ≤ 300 mmHg.

排除标准

  • Vitamin D supplementation in the previous month.
  • Contraindication for vitamin D supplementation: active granulomatosis (sarcoidosis, tuberculosis, lymphoma), history of calcic lithiasis, known hypervitaminosis D or hypercalcemia, known intolerance to vitamin D.
  • Organ failure requiring admission to a resuscitation or high dependency unit.
  • Pregnant women.
  • Participation in another simultaneous clinical trial.

结局指标

主要结局

In-hospital mortality

时间窗: Two weeks

Death during hospitalization

Time to increase in oxygenation

时间窗: 48 hours

Time to increase in SpO2/FiO2 of 50 or greater compared to the baseline SpO2/FiO2)

Duration of hospitalization

时间窗: Two weeks

Length of hospital stay

Clinical status improvement using six category ordinal scale

时间窗: Two weeks

Change in six category ordinal scale. The categories were defined as follows: 1) patient discharged, 2) hospitalization not requiring supplemental oxygen, 3) hospitalization requiring supplemental low-flow oxygen, 4) hospitalization requiring high-flow supplemental oxygen, 5) hospitalization requiring invasive mechanical ventilation, 6) death.

Change in gas exchange

时间窗: Two weeks

Difference between ratio of partial pressure of arterial oxygen (PaO2) to the fraction of inspired oxygen (FiO2) at baseline, and before discharge

次要结局

  • Need for mechanical ventilator or intensive care unit (ICU) support(Two weeks)
  • Change in C-reactive protein (CRP) levels(Two weeks)
  • Occurrence of at least one severe adverse event(Two weeks)
  • Change in serum ferritin levels(Two weeks)
  • Occurrence of secondary infection(Two weeks)
  • Change in Lactate dehydrogenase (LDH) levels(Two weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Neven Sarhan

Lecturer at Faculty of Pharmacy

Misr International University

研究点 (1)

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