Fatty Liver Disease in Obese Children
Primary Purpose
Obesity, Nonalcoholic Fatty Liver Disease, Cardiovascular Disease
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
N-acetyl cysteine 600 mg once/day
N-acetyl cysteine 600mg twice/day
Placebo twice/day
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring fatty liver, obesity, children, oxidative stress, antioxidants
Eligibility Criteria
Inclusion Criteria:
- Age 7 years and older
- NASH confirmed in a previous biopsy
- HbAIc <6.4%
- ALT > 60 U/L or 1.5 times the upper limit of normal
Exclusion Criteria:
- Chronic liver disease including alpha-1-antitrypsin deficiency, Wilson's disease, autoimmune and viral hepatitis
- Medications such as adrenergic β-blockers, steroids and other drugs known to interfere with the measurement of liver enzymes and risk factors for cardiovascular disease
- Heart disease, chronic renal disease, adrenal, hepatic or thyroid dysfunction; active malignancy; and anemia
- History of prior treatment with NAC
- Evidence of hypersensitivity/allergy to NAC
- Alcoholism or drug abuse and smoking
- Inter-current illness over 7 days before the study & surgery in the past 3 mo.
Sites / Locations
- Nemours Children's Clinic/Alfred I duPont Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
N-acetyl cysteine-1
N-acetyl cysteine-2
Placebo
Arm Description
N-acetyl cysteine 600 mg once/day + Placebo once/day for 16 weeks
N-acetyl cysteine 600 mg twice/day for 16 weeks
Placebo twice/day for 16 weeks
Outcomes
Primary Outcome Measures
Change in liver fat (MRI) and ALT levels from baseline and at 16 weeks
The primary outcome will be sustained reduction in ALT level, defined as 50% or less of the baseline level or 40 U/L or less and significant changes in liver fat (MRI) at the end of the study. All measurements of biological factors will be performed in the post absorptive (fasted) state.
Secondary Outcome Measures
Full Information
NCT ID
NCT02117700
First Posted
April 16, 2014
Last Updated
October 13, 2022
Sponsor
Nemours Children's Clinic
1. Study Identification
Unique Protocol Identification Number
NCT02117700
Brief Title
Fatty Liver Disease in Obese Children
Official Title
Effect of N-acetyl Cysteine on Non Alcoholic Fatty Liver Disease in Obese Children
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
April 2015 (Actual)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
December 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nemours Children's Clinic
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Although weight reduction through physical activity-based interventions is the mainstay therapy for nonalcoholic fatty liver disease (NAFLD), its maintenance is difficult and typically unsuccessful. This affirms the extreme need for alternate and/or adjunct therapies. Although convincing data from animal studies and a few adult human studies on the benefits of a natural product, N-acetyl cysteine (NAC), in a variety of liver conditions including NAFLD have emerged, studies in children are scarce. Therefore, the aim of the study is to test the use NAC as an innovative approach to attenuate the progression of NAFD in obese children with biopsy proven NASH. The central hypothesis is that NAC supplementation will reduce liver fat and liver enzymes and ameliorate risk factors of cardiometabolic disease in children with NAFLD.
Detailed Description
Physical activity (PA)-induced weight reduction, the suggested therapy for noalcoholic liver disease (NAFLD), is difficult and its maintenance is typically unsuccessful in children, affirming the acute need for alternative/adjunct therapies. Although few promising approaches have been reported, the benefits are incongruent and mostly marginal. N-acetyl cysteine (NAC), a derivative of the natural amino acid, cysteine, appears to be promising as an adjunct therapy to PA. Animal and a few adult human studies suggest NAC-induced attenuation of liver abnormalities, oxidative stress, insulin resistance and inflammation. The primary aim of the proposal is to determine in obese children with biopsy proven NASH and elevated liver enzymes the effect of NAC at two different doses on liver fat using magnetic resonance imaging (MRI), liver enzymes and risk factors of cardiometabolic disease. We hypothesize that NAC will produce beneficial effect on these parameters.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Nonalcoholic Fatty Liver Disease, Cardiovascular Disease
Keywords
fatty liver, obesity, children, oxidative stress, antioxidants
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Placebo controlled randomized double blind
Allocation
Randomized
Enrollment
14 (Actual)
8. Arms, Groups, and Interventions
Arm Title
N-acetyl cysteine-1
Arm Type
Experimental
Arm Description
N-acetyl cysteine 600 mg once/day + Placebo once/day for 16 weeks
Arm Title
N-acetyl cysteine-2
Arm Type
Experimental
Arm Description
N-acetyl cysteine 600 mg twice/day for 16 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo twice/day for 16 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
N-acetyl cysteine 600 mg once/day
Intervention Description
NAC 600 mg once/day + Placebo once/day for 16 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
N-acetyl cysteine 600mg twice/day
Intervention Description
N-acetyl cysteine 600 mg twice/day for 16 weeks
Intervention Type
Other
Intervention Name(s)
Placebo twice/day
Intervention Description
Placebo capsules twice/day for 16 weeks
Primary Outcome Measure Information:
Title
Change in liver fat (MRI) and ALT levels from baseline and at 16 weeks
Description
The primary outcome will be sustained reduction in ALT level, defined as 50% or less of the baseline level or 40 U/L or less and significant changes in liver fat (MRI) at the end of the study. All measurements of biological factors will be performed in the post absorptive (fasted) state.
Time Frame
Upto 16 weeks
Other Pre-specified Outcome Measures:
Title
Change in Biomarkers of cardiovascular disease from baseline and at 16 weeks
Description
The secondary outcome will be attenuation of abnormal levels of biomarkers of cardiovascular disease such as markers of inflammation, oxidative stress and insulin resistance. All measurements of biological factors will be performed in the post absorptive (fasted) state.
Time Frame
Upto 16 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 7 years and older
NASH confirmed in a previous biopsy
HbAIc <6.4%
ALT > 60 U/L or 1.5 times the upper limit of normal
Exclusion Criteria:
Chronic liver disease including alpha-1-antitrypsin deficiency, Wilson's disease, autoimmune and viral hepatitis
Medications such as adrenergic β-blockers, steroids and other drugs known to interfere with the measurement of liver enzymes and risk factors for cardiovascular disease
Heart disease, chronic renal disease, adrenal, hepatic or thyroid dysfunction; active malignancy; and anemia
History of prior treatment with NAC
Evidence of hypersensitivity/allergy to NAC
Alcoholism or drug abuse and smoking
Inter-current illness over 7 days before the study & surgery in the past 3 mo.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Babu Balagopal, PhD
Organizational Affiliation
Nemours Children's Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nemours Children's Clinic/Alfred I duPont Hospital
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Fatty Liver Disease in Obese Children
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