Prediction of Severity of Liver Disease Non Alcoholic Fatty Liver Disease in Patients With Suspected NAFLD by a 13C Octanoate Breath Test

The Exalenz clinical investigation is a multicenter, non-randomized, blinded, study of the ¹³C-Octanaote breath test (OBT). The OBT is a non-invasive test for evaluation of disease severity in patients with suspected non alcoholic fatty liver disease (NAFLD) The purpose of the study is to demonstrate that the ¹³C-Octanaote Breath Test (OBT) can be used as an aid, in conjunction with other clinical information and medical history, for evaluating disease severity and detecting non alcoholic steatohepatitis(NASH) with a high probability.

Retrospective analysis based on multivariable analysis will determined if and which demographic, clinical and biochemical or imaging techniques data can assist in addition to the data derived from OBT in differentiation of NASH, NAFL and possibly normals.

Study Overview

• Status: Unknown
• Conditions: NAFLD
• Intervention / Treatment: Device: BreathID - Breath Test - 13C Octanoate

• Study Type: Interventional
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Israel
  • Jerusalem, Israel
    • Hadassah Medical Organization

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Adult men or women (>18 years of age)
• Liver -biopsy ( at least 1.7 cm and 4 portal tracts) performed within 6 months of breath test or planned within the next 6 weeks, providing no treatment for liver disease was given between the biopsy and the OBT Any elevation of liver enzymes above the upper limit of normal (any or all of the following: AST,ALT, GGT, Alkaline phosphatase)

• At least one of the features of the metabolic syndrome

  • waist circumference > 100 cm for men, 88 cm for women
  • triglycerides > 150 mg/dl
  • fasting blood sugar > 110 mg/dl
  • HDL cholesterol < 40 mg/dl
  • blood pressure > 130/85 mm Hg
• No other known co-existent liver disease, excluded by appropriate serologic testing

Exclusion Criteria:

• Positive studies for any of the following:
• hepatitis C (PCR)
• hepatitis B (surface antigen or DNA)
• iron saturation > 60% + gene test for hereditary hemochromatosis

• antinuclear antibody at a titer > 1: 160 along with hypergammaglobulinemia and ALT levels>250 U/L

  • Patient has Alpha-1-antitrypsin level below lower limit of normal (< 150 mg/dl)
  • Patient has alcohol consumption > 20 gm/day for women and > 30 gm/day for men
  • Patient is pregnant
  • Patient has been taking known hepatotoxic drugs e.g. (e.g.acebutolol, indomethacin,phenylbutazone,allopurinol,isoniazid,phenytoin,atenolol,ketoconazole,piroxicam,carbamazepine,labetalol,probenecid,cimetidine,maprotiline,pyrazinamide,dantrolene, metoprolol,quinidine,diclofenac, mianserin)• Patients that have had more than 10% reduction in body weight since biopsy
  • Patient with known severe congestive heart failure (LVEF on echocardiogram < 20%)
  • Patient with known severe pulmonary hypertension (By echocardiogram, PAS >45 mmHg)
  • Patient with uncontrolled diabetes mellitus (HA1c>10)
  • Patient with previous surgical bypass surgery
  • Patient with extensive short bowel syndrome(>100 cm)
  • Patient currently receiving total parenteral nutrition
  • Patient is a recipients of any organ transplant
  • Patients that received any anti-viral treatment or any other liver therapy between the time of the biopsy and the breath test.
  • Women who are pregnant
  • Patients with an acute current exacerbation of chronic obstructive pulmonary disease or bronchial asthma.
  • Patient has taken drugs that can interfere with octanoate metabolism or can also cause NAFLD independent of the metabolic syndrome, including: corticosteroids, amiodarone, tetracycline, valproic acid, methotrexate, stavudine, zidovudine.
  • Patients unable or refuse to sign informed consent
  • Patients that based on the opinion of the investigator should not be enrolled into this study
  • Patients that are participating in other clinical trials evaluating experimental treatments or procedures

Study Plan

How is the study designed?

Collaborators and Investigators

• Sponsor: Hadassah Medical Organization
• Collaborators: Meridian Bioscience, Inc.

Study record dates

Study Major Dates

• Study Start: January 1, 2011

Study Registration Dates

• First Submitted: January 10, 2011
• First Submitted That Met QC Criteria: January 20, 2011
• First Posted (Estimate): January 21, 2011

Study Record Updates

• Last Update Posted (Estimate): August 28, 2012
• Last Update Submitted That Met QC Criteria: August 27, 2012
• Last Verified: August 1, 2011

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Digestive System Diseases; Liver Diseases; Fatty Liver; Non-alcoholic Fatty Liver Disease
• Other Study ID Numbers: 0429-10-HMO-CTIL