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临床试验/IRCT20200324046844N1
IRCT20200324046844N1招募中3 期

Effects of ultra dose vitamin D supplementation on remission, morbidity and mortality of ventilator associated pneumonitis (VAP) patients: A Randomized Controlled Trial study.

Shiraz University of Medical Sciences0 个研究点目标入组 42 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
42

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 65 years(—)
性别
All

入选标准

  • Pneumonia Severity Index (PSI) score above 51
  • The level of vitamin D below 20 ng/ml at the admission to the hospital
  • Absence of hypercalcemia at the admission to the hospital (calcium concentration above 10.8 mg/dl)
  • Stable hemodynamic status
  • Not consuming hydrochlorothiazide, digoxin and magnesium containing antacids
  • Absence of history of consuming vitamin D during the past four months with the dose above 1000 units
  • Able to be be fed enterally at the 24 to 48 hours from the admission time
  • Signing the consent form by the family of patients
  • Absence of any of these disease: hyperparathyroidism, nephrolithiasis, sarcoidosis, chronic kidney disease, cirrhosis, metabolic diseases, acquired immune deficiency syndrome (AIDS), cardiovascular disease, diabetes mellitus, cancers and autoimmune diseases
  • Not being pregnant
  • Not involved in other research projects

排除标准

  • Presence of other types of pneumonitis
  • Dying earlier than 7 days of intervention
  • Presence of any condition leading to enteral feeding disruption during the first 5 days of intervention
  • If the supplementation is thought to be hazardous or being forbidden by the general practitioner

研究者

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