Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:10 PM
Ignite Modification Date:
2025-12-24 @ 7:10 PM
NCT ID:
NCT01244503
Eligibility Criteria:
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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01244503
Study Brief:
Protocol Section:
NCT01244503