- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01281059
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.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Jerusalem, Israel
- Hadassah Medical Organization
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
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
Plan de estudios
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Inicio del estudio
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Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
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Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 0429-10-HMO-CTIL
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