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临床试验/NCT02143778
NCT02143778已完成不适用

Clinical Study of the BreathID® LF System to Train the Algorithm for the ¹³C-Methacetin Breath Test (MBT) in Assessment of Portal Hypertension in Patients With Compensated Liver Cirrhosis

Meridian Bioscience, Inc.8 个研究点 分布在 4 个国家目标入组 246 人开始时间: 2014年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
246
试验地点
8
主要终点
CSPH (Clinically Significant Portal Hypertension)

研究概览

简要总结

This study will be used to train an algorithm using Methacetin breath test (MBT) measures and to select a cut-off to determine presence or absence of Clinically Significant Portal Hypertension (CSPH) as defined by Hepatic Venous Gradient Pressure (HVPG) ≥ 10mmHg,

详细描述

The portal pressure leaving the liver is measured by using a balloon catheter before and after a wedge. The difference of the pressure between the wedge and the free is the hepatic venous pressure gradient. Methacetin breath test is hypothesized to also identify CSPH and the agreement to the reference standard (HVPG) will be assessed in this study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • •Adult men or women (>18 years of age)
  • •Known chronic liver disease with cirrhosis
  • •Europe: Indicated to undergo HVPG testing
  • •US: Consented for HVPG
  • •For patients treated with beta blockers: They have to be on a stable dose for at least 6 weeks prior to any study related tasks
  • •For patients who stopped their treatment with beta blockers: Their last dose should be at least 6 weeks prior to any study related tasks

排除标准

  • •Decompensated cirrhosis as clinically defined by the presence of ascites, hepatic encephalopathy, variceal bleeding or hepatorenal syndrome
  • •Renal failure (creatinine > 2.5 mg/dl)
  • •Known acute renal tubular disease Known hypotension (Systolic Pressure <100mmHg)
  • •Hypocoagulablity defined as PT >6 and INR >2.
  • •Congestive heart failure (assessed clinically as NIHA >2)
  • •Known pulmonary hypertension (right ventricular systolic pressure > 45 mm Hg)
  • •Uncontrolled diabetes mellitus (HBA1C >9.5gr%)
  • •Concurrent prednisone or immunosuppressive treatment, if therapy and/or response to treatment are not stable for at least 3 months.
  • •Documented or suspected hepatocellular carcinoma
  • •Gastric bypass surgery or extensive small bowel resection
  • •Total parenteral nutrition
  • •Any organ transplant recipient
  • •Pregnant or breast feeding
  • •Allergy to acetaminophen and/or other related medications
  • •Documented drug-related concurrent hepatotoxicity or drug-related silent steatosis or drug-related fibrosis (e.g. amiodarone, methotrexate and tamoxifen)
  • •Uncontrolled malabsorption or diarrhea
  • •Documented non-cirrhotic PHT, partial / complete portal venous occlusion, hepatic venous occlusion, previous PHT surgery, or placement of a transjugular intrahepatic portosystemic shunt (TIPS)
  • •Primary or secondary biliary cirrhosis, primary or secondary sclerosing cholangitis, hepatic sarcoidosis, or other cholestatic disorders
  • •Subjects unable to perform the MBT within 7 days of HVPG procedure.
  • •Subject should not have taken any of the following for at least 48 hours prior to the breath test: Acyclovir , allopurinol, amiodarone, carbamazepine, cimetidine, ciprofloxacin, daidzein, (herbal) disulfiram, echinacea, enoxacin, famotidine, fluvoxamine, methoxsalen, mexiletine, montelukast, norfloxacin, phenylpropanolamine, phenytoin, propafenone, rifampin, terbinafine, ticlopidine, thiabendazole, verapamil, zileuton or oral contraceptives or any medication that might interfere with Methacetin metabolism or might affect CYP 1A2
  • •Subject should not have taken amiodarone or statins within the last 30 days prior to the breath test or HVPG procedure

研究组 & 干预措施

Compensated cirrhotic patients

Experimental

A methacetin breath test will be performed on patients who are undergoing the HVPG procedure due to their clinical indication of compensated cirrhosis.

干预措施: Methacetin Breath Test (Device)

结局指标

主要结局

CSPH (Clinically Significant Portal Hypertension)

时间窗: 1 hour

Clinically significant portal hypertension is defined as Hepatic Venous Pressure Gradient (HVPG)\>=10mmHg, whereby the portal pressure leaving the liver is measured by using a balloon catheter before and after a wedge. The difference of the pressure between the wedge and the free is the hepatic venous pressure gradient. Methacetin breath test is hypothesized to also identify CSPH and the agreement to the reference standard (HVPG) will be assessed in this study.

次要结局

  • Hepatic Venous Pressure Gradient (HVPG)>=12; Severe Portal Hypertension (SPH)(1 hour)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (8)

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