跳至主要内容
临床试验/CTRI/2020/09/027527
CTRI/2020/09/027527招募中未知

Efficacy of Vitamin C on AKI Outcomes in Critically Ill Cirrhotics With Multidrug-resistant Bacterial Infections- A Randomized Controlled Trial

Institute of Liver and Biliary Sciences0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中

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

入选标准

  • Critically ill cirrhotics with MDR infections

排除标准

  • 1.Patients with age less than 18 years
  • 2.Known severe cardiopulmonary disease (structural or valvular heart disease, coronary artery disease, COPD)
  • 3.Patients in DIC with platelets < 20,000 and INR > 4 or active bleeding
  • 4.Limitations of care (defined as refusal of cardiovascular and respiratory support modes) including do not intubate (DNI) status
  • 5.Current hospitalization > 15 days for patients with nosocomial acquisition of MDR at time of randomization
  • 6.Known allergy or contraindication to vitamin C (including previously or currently diagnosed primary hyperoxaluria and/or oxalate nephropathy, or known/suspected ethylene glycol ingestion,
  • 7.Known glucose-6-phosphate dehydrogenase (G6PD) deficiency)
  • 8.Use of vitamin C at a dose of > 1 gram daily within the 24 hours preceding first episode of qualifying organ dysfunction during a given ED or ICU admission
  • 9.Patients with HCC (beyond Milan) or extrahepatic malignancies
  • 10.Patients with HVOTO or EHPVO
  • 11.Pregnancy or active breastfeeding
  • 12.Current participation in another interventional research study
  • 13.Active or history of kidney stone
  • 14.History of chronic kidney disease or intrinsic kidney disease
  • 15.Patients already on maintenance hemodialysis prior to presentation
  • 16.Patients with refractory septic shock or hypoxemia (Pa02/Fio2 ratio <100)
  • 17.Extremely moribund patients with an expected life expectancy of less than 24 hours
  • 18.Failure to provide informed consent
  • 19.Patients with retroviral infection
  • 20.Patients with acute on chronic liver failure (APASL definition)
  • 21.Patients with urinary tract infection

研究者

相似试验