Evaluating Carbocisteine for Nonalcoholic Fatty Liver Disease

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to assess the safety and efficacy of Carbocisteine in treating patients with Nonalcoholic Fatty Liver Disease (NAFLD). The study involves administering Carbocisteine alongside lifestyle interventions such as physical activity and calorie restriction. Participants will be adult patients diagnosed with fatty liver through ultrasound, and the trial will monitor their response to the treatment. The goal is to determine if Carbocisteine can improve liver health in this patient population.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Either male or female adult patients (\>18 years) with fatty liver diagnosis by using upper abdominal ultrasound echography

Exclusion Criteria:

* Pregnant and/or lactating women
* Excessive alcohol use (defined as an average alcohol intake \> 30 g per day in men and \> 20 g per day in women)
* Other etiology of chronic liver diseases such as viral hepatitis, drug-induced hepatitis, autoimmune hepatitis.
* patients suffering from chronic kidney disease, and hyper/hypoparathyroidism
* Hypersensitivity to carbocistiene.

Where it's running

• Tanta Unuversity
  Tanta, Egypt Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.