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BreathID Multi-center HCV Liver Breath Test Study

Primary Purpose

Hepatitis C

Status
Terminated
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
MBT and BreathID
Sponsored by
Meridian Bioscience, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Hepatitis C focused on measuring HCV (Hepatitis C Virus), MBT (Methacetin Breath Test), Hepatitis C Virus Patients

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: i. Patients with a confirmed diagnosis of Chronic HCV only : ii. Patients for whom a liver biopsy has been performed within the last 90 days or who will undergo a liver biopsy within the time frame of the study. Exclusion Criteria: i. Severe congestive heart failure. ii. Severe pulmonary hypertension. iii.Chronic renal insufficiency defined by a serum creatinine above the limits of normal. iv. Uncontrolled diabetes mellitus (need definition).v.Any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication. vi.Proven or suspected hepatocellular carcinoma. vii. Previous surgical bypass surgery for morbid obesity viii.Extensive small bowel resection. ix.Patients currently receiving total parenteral nutrition x.Recipients of any organ transplant. xi.Other co-existent liver disease.

Sites / Locations

  • Mount Sinai School of Medicine
  • Baylor College of Medicine
  • U.S. Dept. of Veteran Affairs, Hunter Holmes McGuire Medical Center
  • Virginia Commonwealth Univeristy
  • Hadassah Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MBT

Arm Description

C13 methacetin dissolved in water to be ingested after breath baseline collected. Metabolism to measured in real time.

Outcomes

Primary Outcome Measures

Correlation of Breath Test (MBT) to Fibrosis
13 C Lebeled substrate is metabolized by Liver and reflects liver function. It is hypothesized that this correlated to liver fibrosis

Secondary Outcome Measures

Full Information

First Posted
July 10, 2006
Last Updated
December 19, 2022
Sponsor
Meridian Bioscience, Inc.
Collaborators
Icahn School of Medicine at Mount Sinai, Baylor College of Medicine, Virginia Commonwealth University, Hadassah Medical Organization, US Department of Veterans Affairs
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1. Study Identification

Unique Protocol Identification Number
NCT00350714
Brief Title
BreathID Multi-center HCV Liver Breath Test Study
Official Title
Validation of a Breath Test for Assessment of Liver Fibrosis in Patients With Chronic Hepatitis C Viral Infection
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Terminated
Why Stopped
Due to FDA comments, protocol changed; new trial will be proposed shortly
Study Start Date
July 2006 (undefined)
Primary Completion Date
February 2007 (Actual)
Study Completion Date
February 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Meridian Bioscience, Inc.
Collaborators
Icahn School of Medicine at Mount Sinai, Baylor College of Medicine, Virginia Commonwealth University, Hadassah Medical Organization, US Department of Veterans Affairs

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this study is to validate the BreathID 13C-methacetin breath test (MBT) as a non-invasive simple-to-use metabolic test, which could be utilized to detect severe liver fibrosis (>2 in METAVIR) in patients with chronic HCV liver disease.The test is a breath-test using a free-standing device (BreathID®) that measures metabolization of a 13C-labeled substrate (13C-methacetin) in real time.
Detailed Description
Percutaneous liver biopsy has been utilized for decades to assess the severity of chronic HCV liver disease. During this procedure a core sample of liver is obtained and examined histologically for the presence of inflammation, fibrosis and other features characteristic of specific liver disorders. Several grading systems have been developed over the past 2 decades to quantify the overall severity of the liver biopsy specimen. Although liver biopsy is the gold standard by which to assess liver disease severity, the procedure has significant limitations. Liver biopsy is a costly, invasive procedure with risks for morbidity and mortality and may cause some discomfort to the patient. Percutaneous liver biopsy is associated with potential complications, including bleeding (1%-3%), pain (20%-30%), bile peritonitis (<1%), pneumothorax (<1%), punctured viscera (<1%), and death. In addition, liver biopsy and examination of liver histology is subject to sampling variation and the manner by which these findings are evaluated and reported by individual pathologists. Breath testing with 13C-labeled substrates provide a safe, non-invasive means for evaluating hepatic metabolism that is correlated with liver histology. 13C is a stable, non-radioactive isotope, which can by incorporated into a specific location within a test substrate so that it would be released when the compound is metabolized by the liver. Ideally, the 13C-compound would need to be administered orally, rapidly absorbed, exclusively metabolized by the liver metabolism and 13C would be measured in exhaled breath within 20-30 minutes. Hepatic metabolism of the compound is assessed by measuring the ratio of 13C/12C in exhaled breath. The ability to detect, differentiate and quantify 13C and 12C in exhaled CO2 has been greatly facilitated by the recent development of the BreathID® collection system and analyzer unit. The compound selected for this study will be 13C-methacetin. Methacetin meets all of the qualifications for an excellent substrate for liver breath tests. It is a non-toxic small molecule. 13C can be synthesized into a key location within this agent. It can be administered orally in solution. It is rapidly absorbed and metabolized by hepatic microsomes and this process releases CO2 as a by-product in exhaled breath. No reports of any complications or side effects using this substance have been reported. 13C-methacetin is rapidly absorbed and metabolized by healthy liver cells into acetaminophen and 13CO2. The resultant CO2 can be measured in the exhaled breath. The amount of metabolized methacetin indicates the capability of the liver to accomplish one of its main physiological tasks and has been shown to correlate with liver fibrosis and cirrhosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C
Keywords
HCV (Hepatitis C Virus), MBT (Methacetin Breath Test), Hepatitis C Virus Patients

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MBT
Arm Type
Experimental
Arm Description
C13 methacetin dissolved in water to be ingested after breath baseline collected. Metabolism to measured in real time.
Intervention Type
Other
Intervention Name(s)
MBT and BreathID
Intervention Description
75 mg methacetin (c13 labelled) dissolved in 150 cc water ingested and breath collected before and after ingestion.
Primary Outcome Measure Information:
Title
Correlation of Breath Test (MBT) to Fibrosis
Description
13 C Lebeled substrate is metabolized by Liver and reflects liver function. It is hypothesized that this correlated to liver fibrosis
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: i. Patients with a confirmed diagnosis of Chronic HCV only : ii. Patients for whom a liver biopsy has been performed within the last 90 days or who will undergo a liver biopsy within the time frame of the study. Exclusion Criteria: i. Severe congestive heart failure. ii. Severe pulmonary hypertension. iii.Chronic renal insufficiency defined by a serum creatinine above the limits of normal. iv. Uncontrolled diabetes mellitus (need definition).v.Any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication. vi.Proven or suspected hepatocellular carcinoma. vii. Previous surgical bypass surgery for morbid obesity viii.Extensive small bowel resection. ix.Patients currently receiving total parenteral nutrition x.Recipients of any organ transplant. xi.Other co-existent liver disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Doug Dieterich, MD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John M Vierling, MD
Organizational Affiliation
Baylor College of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mitchell Shiffman, MD
Organizational Affiliation
Virginia Commonwealth University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Maya Margalit, MD
Organizational Affiliation
Hadassah Medical Organization
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Douglas M. Heuman, M.D.
Organizational Affiliation
U.S. Dept. of Veteran Affairs, Hunter Holmes McGuire Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10029-6574
Country
United States
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
U.S. Dept. of Veteran Affairs, Hunter Holmes McGuire Medical Center
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23249-0001
Country
United States
Facility Name
Virginia Commonwealth Univeristy
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23284
Country
United States
Facility Name
Hadassah Medical Center
City
Jerusalem
Country
Israel

12. IPD Sharing Statement

Citations:
Citation
O. Goetze; N. Selzner; A. Grau; M. Fried; T. Gerlach; B. Muellhaupt 13C-Methacetin Breath Test by Online Molecular Correlation Spectroscopy Compared to APRI and Liver Biopsy for the Assessment of Fibrosis in Chronic Hepatitis C , S1047. Abstarct presented at DDW 2006
Results Reference
result
Links:
URL
http://www.breathid.com
Description
Website of BreathID whose device will be used in this study

Learn more about this trial

BreathID Multi-center HCV Liver Breath Test Study

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