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Efficacy of N-Acetylcysteine in Improving/Normalizing ALT & AST in Patients of NAFLD

Efficacy of N-Acetylcysteine in Improving/Normalizing ALT & AST in Patients of NAFLD

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05576428
Enrollment
100
Registered
2022-10-12
Start date
2022-11-01
Completion date
2023-05-15
Last updated
2022-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NAFLD

Brief summary

Currently researches are focusing on the effect of antioxidants in the treatment of non-alcoholic fatty liver disease (NAFLD). Since N-acetyl cysteine (NAC) has been proven to have antioxidant and anti-inflammatory properties, therefore, we will conduct this study to determine the effect of NAC in patients of NAFLD with raised liver enzymes.

Detailed description

The prevalence of non-alcoholic fatty liver disease (NAFLD) is increasing globally, and presents a challenge for the medical community since it has no FDA approved treatment. An important feature of non-alcoholic fatty liver disease (NAFLD) is hepatic steatosis leading to hepatic dysfunction . It has been reported that NAFLD patients with increased liver enzymes have a greater risk of developing complications like cirrhosis and end-stage liver disease. since N-acetyl cysteine (NAC) has been proven to have antioxidant and anti-inflammatory properties, therefore, we will conduct this study to determine the effect of NAC in patients of NAFLD with raised liver enzymes (ALT, AST). Patients presenting with ultrasound showing fatty liver with raised liver enzymes will be recruited. They will be randomized into two groups (group A and group B). The odd number patients will be allocated group A and even number patients will be allocated to group B. Group A: patients in this group will be advised to follow a diet plan & daily 20 minutes brisk walking. Group B: Patients in this group will be given NAC 200mg BD along with diet plan & exercise. This drug will be provided to the patients by the investigators free of cost. The liver function tests and side effects of NAC will be followed at 12 weeks .

Interventions

BEHAVIORALDiet and exercise

diet and exercise in patients of NAFLD

DRUGNAC with diet and exercise

NAC with diet and exercise in patients of NAFLD

Sponsors

Dow University of Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* • Patients of both genders between the ages of 20 years and 60 years, giving consent to be included in the study. * Patients having fatty liver on ultrasound with raised ALT and AST levels

Exclusion criteria

* • Patients having other causes of steatosis eg, excessive alcohol consumption, * Patients taking steatogenic medications such as, methotrexate , corticosteroids etc. * Patients suffering from other diseases that could increase ALT levels eg. Viral hepatitis, HIV, autoimmune liver diseases, infiltrative liver diseases. * Patients suffering from malignancies. * Patients who are not compliant to the medicine. * Pregnant and nursing females

Design outcomes

Primary

MeasureTime frameDescription
Change in Alanine transaminase,aspartate aminotransferase12 weeksChange in Alanine transaminase,aspartate aminotransferase

Secondary

MeasureTime frameDescription
Side Effects of NAC12 weeksSide Effects of NAC

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026