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临床试验/NCT04353193
NCT04353193Unknown4 期

Hemodynamic Profile of Terlipressin and Octreotide in Patients With Cirrhosis and Portal Hypertension. A Randomised, Single Blinded Clinical Trial.

Juan A. Arnaiz1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2020年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
36
试验地点
1
主要终点
Change in HVPG

研究概览

简要总结

Clinical trial to compare the effects of terlipressin and octreotide in the reduction of portal hypertension measured as hepatic venous pressure gradient (HVPG) in patients with liver cirrhosis

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

single blind

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: 18-75 years old.
  • Liver Cirrhosis
  • Portal hypertension
  • Stable disease in the absence of vasoactive agents
  • Signed informed consent form

排除标准

  • Patients on medications that can prolong QT interval
  • Patients with HCC not fulfilling Milan criteria for transplant
  • Grade II-IV hepatic encephalopathy
  • GI bleeding in the last 10 days
  • Child-Pugh C above 12 points
  • Bacterial infection in the last 10 days
  • HVPG <12mmHg
  • Plasma sodium <130mmol/l
  • Serum creatinine >2mg/dl
  • Serum bilirubin >5mg/dl
  • Uncontrolled cardiovascular disease
  • HIV infection
  • Extra hepatic malignancies
  • Heart failure NYHA Grade III/IV, COPD GOLD>2
  • Morbid obesity
  • Coronary heart disease or intestinal ischemia
  • Pregnancy or breastfeeding

研究组 & 干预措施

Terlipressin IV bolus

Experimental

Terlipressin 1mg IV bolus

干预措施: Terlipressin (Drug)

Terlipressin IV continuous infusion

Experimental

Terlipressin by IV continuous infusion at a rate of 2mg/day (max 4mg/day) during 2 hours

干预措施: Terlipressin (Drug)

Octreotide IV bolus plus continuous infusion

Experimental

Octreotide 50mcg IV bolus plus continuous infusion at a rate of 50mcg/h during 2 hours

干预措施: Octreotide (Drug)

结局指标

主要结局

Change in HVPG

时间窗: 30 minutes, 1 hour and 2 hours

次要结局

未报告次要终点

研究者

发起方
Juan A. Arnaiz
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Juan A. Arnaiz

MD

Hospital Clinic of Barcelona

研究点 (1)

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