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临床试验/KCT0000102
KCT0000102招募中未知

A Randomized, Multi-center, Phase IV Open-label Study to Evaluate the Long-term Effect of Carvedilol versus Propranolol on Reduction in Portal Pressure in Patients with Cirrhosis

Hanyang University Guri Hospital0 个研究点目标入组 130 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
130

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
20(Year) 至 70(Year)(—)
性别
All

入选标准

  • (1) cirrhosis
  • (2) severe portal hypertension (hepatic venous pressure gradient > 12mmHg)
  • (3) F2/F3 varices or endoscopic treatment of large esophageal varices at least 3 months old the last time
  • (4) Child-Pugh score < 12
  • (5) not taking patients beta-blocker, ACE inhibitor, nitrate within 1 month

排除标准

  • (1) systolic blood pressure < 90 mmHg, baseline heart rate < 55/min
  • (2) refractory ascites, hepatic encephalopathy, hepatorenal syndrome
  • (3) hepatocellular carcinoma
  • (4) presence of severe systemic illness
  • (5) history of gastric variceal hemorrhage
  • (6) contraindication of beta-blocker
  • (7) serum jaundice > 10 mg/dL
  • (8) srum creatinine = 1.2 mg/dL
  • (9) history of shunt or TIPS
  • (11) pregnancy
  • (12) allergy to beta-blocker or alpha-blocker
  • (13) unwilling to sign inform consent
  • (14) Clinical investigator have determined that patient is difficult to perform the clinical trial.

研究者

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