CTRI/2022/03/041109招募中未知
Efficacy and Safety of Vasopressin Versus Terlipressin as a Second Vasopressor in Critically Ill Cirrhotics With Septic Shock- the VITEL-C Trial.
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
- •1) Age 18-70 yrs
- •2) An informed consent from the patient or relative
排除标准
- •1.Age <18 years and > 70 years
- •3.Severe sepsis requiring higher dose of noradrenaline ( >1mcg/Kg/min)
- •4.Myocardial dysfunction, Coronary artery disease, Arrhythmias
- •5.Peripheral Vascular disease
- •6.Gut Paralysis
- •7.Acute on chronic liver failure (ACLF)
- •8.Hepato-cellular carcinoma (HCC), intrahepatic or extrahepatic malignancy
- •9.Complete portal vein thrombosis
- •10.Hepatic vein outflow tract obstruction (HVOTO)
- •11.Pregnancy
- •12.Patients with Pa02/FiO2 ratio <150
- •15.Severe coagulopathy - platelets <20,000 and INR > 4
- •16.Active Bleed or DIC
- •17.Patients already on terlipressin or vasopressin in the last 48 hours
- •18.Extremely moribund patients with an expected life expectancy of less than 24 hours
- •19.Failure to give informed consent from family members.
- •20.Patient enrolled in other clinical trial
研究者
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