The SHUNT-V Study for Varices
- Conditions
- Chronic Liver Disease
- Interventions
- Combination Product: HepQuant SHUNT Liver Diagnostic Test
- Registration Number
- NCT03583996
- Lead Sponsor
- HepQuant, LLC
- Brief Summary
The purpose of this study is to validate the Disease Severity Index (DSI) from the HepQuant SHUNT Liver Diagnostic Kit (Test) for likelihood of large esophageal varices.
- Detailed Description
The purpose of this study is to validate the Disease Severity Index (DSI) from the HepQuant SHUNT Liver Diagnostic Kit (Test) for likelihood of large esophageal varices. The Hepatitis C Antiviral Long-term Treatment against Cirrhosis (HALT-C) Trial training dataset demonstrated that the DSI 18.3 had sensitivity 95%, specificity 54%, positive predictive value (PPV) 19%, negative predictive value (NPV) \>99%, negative likelihood ratio (NLR) 0.09, and positive likelihood ratio (PLR) 2.09 for large varices. To validate DSI 18.3 as a cutoff for large varices, we will enroll 420 subjects with chronic liver disease (CLD) of mixed etiologies from 15 to 25 US clinical centers (CLD Validation dataset). The target prevalence of large varices is ≥20%. Each subject will have been scheduled for an esophago-gastro-duodenoscopy (EGD) as part of their standard of care for either variceal or non-variceal indications. Enrolled subjects will undergo standard clinical assessment, laboratory tests, and the HepQuant SHUNT Test. The EGD will be performed within 6 weeks following the HepQuant SHUNT Test. The relationship of DSI to large varices will be analyzed by univariate and multivariate logistic regression analyses, area under the receiver operating characteristic curve (AUROC), and linear and nonlinear regression and correlation coefficients. Diagnostic performance of the DSI cutoff will be defined in the CLD Validation dataset and validated for likelihood of large esophageal varices. The validated DSI cutoff will identify subjects who are either unlikely or likely to have large esophageal varices.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 306
- Ability to have a peripheral venous catheter for administration of the 13C cholate
- Ability to take the oral dose of d4-cholate
- Ability to hold morning doses of medications for the 90-minute duration of the HepQuant SHUNT Test
- Meets the protocol defined criteria for CLD in addition to having the diagnoses of CLD for >6 months
- Is scheduled, or in the process of being scheduled, for a standard of care EGD
- Unable to give informed consent
- Unable to obtain venous access for administration of intravenous cholate
- Unable to absorb orally-administered cholate
- Known hypersensitivity to human serum albumin
- Known hypersensitivity to any of the components of the HepQuant SHUNT Liver Diagnostic Kit
- Acute hepatitis or Acute Liver Failure
- Acute drug-induced liver disease (DILI)
- Noncirrhotic causes for portal hypertension and varices
- Ongoing active alcoholic hepatitis
- Child-Pugh class C defined by Child-Pugh score 10 or higher
- Dialysis
- Active infection or febrile illness within the last month
- Documented history of esophageal or gastric variceal hemorrhage
- Documented history of treatment of esophageal varices
- Documented history of endoscopic findings of large esophageal varices
- Hepatocellular carcinoma beyond Milan or University of California, San Francisco (UCSF) criteria
- Thrombosis of main portal vein
- Liver transplant recipient
- Pregnancy
- Women who are breast-feeding
- Serious intercurrent medical or surgical illness, such as acute myocardial infarction, acute cerebral hemorrhage, sepsis, or other immediate life-threatening illness
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Open Label HepQuant SHUNT Liver Diagnostic Test All subjects receive HepQuant SHUNT Liver Diagnostic Test within 42 days of the scheduled EGD. Test includes 20mg of 13C Cholate mixed with Albumin via IV push, and 40mg of d4 Cholate mixed with juice orally, both doses given simultaneously one time.
- Primary Outcome Measures
Name Time Method Disease Severity Index (DSI) Less Than/Equal to 18.3 to Rule Out Large Varices 1 day The primary objective of this study is to measure the subjects' liver function using DSI ≤18.3 for those that are not likely to have large esophageal varices.
- Secondary Outcome Measures
Name Time Method DSI and Probability of Large Esophageal Varices 1 day Logistic regression analysis of DSI as predictor of large varices
Trial Locations
- Locations (26)
Methodist Dallas Liver Center
🇺🇸Dallas, Texas, United States
University of WA
🇺🇸Seattle, Washington, United States
Accel Research Sites
🇺🇸Orange City, Florida, United States
Arizona Liver Health
🇺🇸Chandler, Arizona, United States
Nature Coast Clinical Research
🇺🇸Inverness, Florida, United States
Clinical Trials of Texas
🇺🇸San Antonio, Texas, United States
Mayo Clinic, Rochester
🇺🇸Rochester, Minnesota, United States
Southern CA Research Center
🇺🇸Coronado, California, United States
California Liver Research Institute
🇺🇸Pasadena, California, United States
Peak Gastroenterlogy Associates
🇺🇸Colorado Springs, Colorado, United States
Inland Empire Liver Foundation
🇺🇸Rialto, California, United States
Mayo Clinic, Jacksonville
🇺🇸Jacksonville, Florida, United States
Gastroenterology Health Partners, PLLC
🇺🇸New Albany, Indiana, United States
Tandem Clinical Research
🇺🇸Marrero, Louisiana, United States
Gastroenterology Associates of Pensacola
🇺🇸Pensacola, Florida, United States
Digestive Disease Associates
🇺🇸Catonsville, Maryland, United States
Univ of Pennsylvania Hospital
🇺🇸Philadelphia, Pennsylvania, United States
Lucas Research (Diabetes & Endocrinology Consultants, PC)
🇺🇸Morehead City, North Carolina, United States
St Louis University
🇺🇸Saint Louis, Missouri, United States
Baylor, Scott & White
🇺🇸Dallas, Texas, United States
Intermountain Healthcare
🇺🇸Murray, Utah, United States
Bon Secours, Newport News
🇺🇸Newport News, Virginia, United States
Gastroenterology Consultants of SW VA
🇺🇸Roanoke, Virginia, United States
PMG Research
🇺🇸Winston-Salem, North Carolina, United States
Ralph H Johnson Veterans Affairs Medical Center
🇺🇸Charleston, South Carolina, United States
Bon Secours, Richmond
🇺🇸Richmond, Virginia, United States