Detection of Hepatocellular Carcinoma (HCC) With Octanoate Breath ID Test Compared to MRI

Phase 2

Terminated

• Conditions: Chronic Liver Disease; Hepatocellular Carcinoma (HCC)
• Interventions: Drug: 13C Sodium Octanoate

• Registration Number: NCT01433016
• Lead Sponsor: Meridian Bioscience, Inc.

Brief Summary

The Exalenz clinical investigation is a multicenter, non-randomized, study of the ¹³C-Octanoate Breath Test (OBT). The present study is a feasibility trial, which aims to evaluate the capability of the OBT measurement to differentiate between presence and absence of HCC determined by Magnetic Resonance Imaging (MRI) in patients with chronic liver disease.

Detailed Description

The Octanoate Breath Test (OBT) developed by Exalenz is performed by the BreathID System consists of the BreathID device and a test kit containing a nasal cannula, a calibration gas container and a non-radioactive isotope ¹³C- Octanoate solution, and measures and computes the ratio between ¹³CO2 and 12CO2 in the patient's exhaled breath.

This study's aim is to provide data on this novel system to dynamically and accurately assess liver function at the bed side. It is hoped that the system will provide prognostic information faster than is achieved at present with traditional methods. It is hypothesized that in the future the OBT may have an impact on decision making and clinical practice in this group of HCC patients, allowing a greater chance for proper management and hence survival.

Study Timeline

• Study First Submitted: 2011-09-11
• Study First Submitted QC: 2011-09-12
• Study First Posted: 2011-09-13
• Study Start: 2011-11
• Primary Completion: 2012-05
• Study Completion: 2013-05
• Results First Submitted: 2014-02-11
• Results First Submitted QC: 2014-02-27
• Results First Posted: 2014-04-07
• Status Verified: 2022-12
• Last Update Submitted: 2022-12-19
• Last Update Posted: 2022-12-20

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Any patients with chronic liver disease at risk for HCC.
• Age > 18 years.
• Patient has an MRI result (positive or negative for HCC) up to 3 months prior to recruitment or will be scheduled for an MRI during the trial period.
• Patient is naïve to any HCC treatment.

Exclusion Criteria

• Underwent any RFA or TACE or Oral HCC treatments.
• Portal vein thrombosis.
• Prior TIPS placement.
• Severe congestive heart failure (LVEF on echocardiogram < 20%).
• Severe pulmonary hypertension (By echocardiogram, PAS >45 mmHg).
• Uncontrolled diabetes mellitus (HBA1C >9.5%).
• Any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication.
• Previous surgical bypass surgery for morbid obesity (BMI >45).
• Extensive small bowel resection.
• Patients currently receiving total parenteral nutrition if they have contraindications to oral drugs.
• Women who are pregnant or breast feeding.
• 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.
• Patient, based on the opinion of the investigator, should not be enrolled into this study.
• Patient is unable or unwilling to sign informed consent.
• Patients that are participating in other clinical trials evaluating experimental treatments or procedures

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Octanaote Breath Test	13C Sodium Octanoate	A Octanoate breath test will be performed on this single arm population

Primary Outcome Measures

Name	Time	Method
PDR Peak	At study day one after one hour	PDR peak - the rate at which the 13C labeled substrate is metabolized, percentage dose recovery.

Trial Locations

Locations (1)

Toronto General Hospital; 🇨🇦 Toronto, Ontario, Canada