Cincinnati, Ohio 45229


Purpose:

The goal of this study is to determine effective treatment and identify diagnostic biomarkers for Nonalcoholic steatohepatitis (NASH). Individuals that take part in the study will be participating in either a weight loss surgery (WLS) group or a comprehensive lifestyle intervention (CLI) group. People in the WLS group will receive vertical sleeve gastrectomy (VSG). The CLI group will receive dietary, activity and behavioral interventions provided by trained study staff.


Study summary:

The investigators have designed a rigorously controlled study designed to evaluate NASH outcomes in two parallel cohorts: 1) severely obese adolescents with NASH who have chosen to undergo WLS (specifically VSG) for clinical indications compared to 2) a control group of severely obese adolescents with NASH enrolled in a CLI offered as part of this study. The study will provide the best evidence to date of the effectiveness of WLS and CLI in treating NASH in adolescents with body mass index (BMI) ≥ 35 kg/m2. The investigators will also concurrently collect health-care utilization data to enable subsequent cost-effectiveness analyses (CEA) to evaluate the cost-effectiveness of WLS vs. CLI intervention in severely-obese adolescents with NASH. If the investigators' data support our hypothesis that WLS yields superior results, this will set the stage for randomized studies (if needed) and translational studies of weight loss-independent biological mechanism(s) unique to WLS, which may include specific changes in bile acid signaling and in the intestinal microbiome. The latter would facilitate developing novel pharmacotherapies accessible to younger or less obese children with NASH to whom WLS is not applicable. Cumulatively, this study has the potential to yield significant improvements in medical and quality of life (QOL) outcomes for a large proportion of pediatric patients with NASH and to reduce long term health care costs by identifying effective treatment options and decreasing progression to cirrhosis and end-stage liver disease.


Criteria:

Inclusion Criteria: - Adolescents ages 13-19 years (range as defined by World Health Organization). - BMI ≥ 35 to 60 kg/m2 (minimum BMI per current guidelines for WLS in adolescents). An upper limit of BMI was set to avoid rare outliers in BMI. - Meet current standard of care eligibility criteria for adolescent WLS. - Liver biopsy for clinical indication to evaluate for NASH within 90 days of enrollment. Biopsy must confirm definite or borderline NASH with a minimum histological NASH Activity Score of ≥ 3. - No evidence of any other liver disease by history, screening tests or histological evaluation. - Written informed consent from parent/legal guardian and informed assent from the adolescent Exclusion Criteria: - Evidence of other chronic liver disease: autoimmune hepatitis; hepatitis B; hepatitis C; hemochromatosis; alpha-1-antitrypsin (A1AT) deficiency; Wilson disease; use of medications known to cause fatty liver for > 2 consecutive weeks in past year (i.e. systemic glucocorticoids, tetracycline, anabolic steroids, valproic acid); alcohol intake >10 gm/day females & >20 gm/day males. - Non-compensated liver disease with any of the following: hemoglobin <10 g/dL; white blood cell count <3,500 cells/mm3, platelet count <130,000 cells/mm3 of blood, direct bilirubin >1.0 mg/dL, total bilirubin >3 mg/dL, albumin <3.2 g/dL, international normalized ratio (INR) >1.4 - Active psychiatric disorder that would prevent eligibility for WLS or impede adherence to CLI, including clinically significant depression (hospitalization or suicidal ideation) in past 12 months. - Any medical condition preventing eligibility for WLS including but not limited to micronutrient deficiencies (e.g. iron) refractory to medical therapy or inflammatory bowel disease. - Poorly controlled Type 2 diabetes mellitus (T2DM) defined as hemoglobin A1C (HgbA1c) > 9%. - Use of high dose vitamin E (>400 IU per day) or other medications which could alter NASH histology at any time within 3 months prior to baseline liver biopsy or during the trial. - Inability or failure to provide informed assent/consent - Current enrollment in another clinical trial or receipt of an investigational study drug within 6 months prior to the baseline liver biopsy - Any female who is currently nursing, planning a pregnancy, known or suspected to be pregnant, or has a positive pregnancy screen - Inability to travel to study site at intervals necessary for clinical interventions (CLI or WLS). - Prior history of WLS.


NCT ID:

NCT02412540


Primary Contact:

Principal Investigator
Stavra Xanthakos, MD
Children's Hospital Medical Center, Cincinnati

Kimberlee Bernstein, BS
Phone: (513)636-4406
Email: Kimberlee.Bernstein@cchmc.org


Backup Contact:

Email: Stavra.Xanthakos@cchmc.org
Stavra Xanthakos, MD
Phone: (513)636-4680


Location Contact:

Cincinnati, Ohio 45229
United States

Kimberlee Berstein, BS
Phone: 513-636-4406
Email: Kimberlee.Bernstein@cchmc.org

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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