Actively Recruiting

Phase 2
Age: 18Years - 65Years
All Genders
NCT06863376

Evaluating the Safety and Efficacy of Carbocisteine in the Treatment of Nonalcoholic Fatty Liver Disease Patients

Led by Tanta University · Updated on 2026-05-04

46

Participants Needed

1

Research Sites

111 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Nonalcoholic fatty liver disease (NAFLD) is a global public health concern, and the leading cause of chronic liver disease, especially in developed countries. NAFLD is characterized by lipid accumulation in the liver not attributed to other causes. Lifestyle interventions, including dietary modification and exercise, remain the cornerstone of NAFLD treatment. Pharmacological treatments aimed primarily at improving liver disease should generally be limited to those with biopsy-proven NASH and fibrosis.

CONDITIONS

Official Title

Evaluating the Safety and Efficacy of Carbocisteine in the Treatment of Nonalcoholic Fatty Liver Disease Patients

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult male or female patients older than 18 years
  • Diagnosis of fatty liver confirmed by upper abdominal ultrasound
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding women
  • Excessive alcohol use (more than 30 g/day for men, more than 20 g/day for women)
  • Other chronic liver diseases such as viral hepatitis, drug-induced hepatitis, or autoimmune hepatitis
  • Chronic kidney disease
  • Hyperparathyroidism or hypoparathyroidism
  • Allergy or hypersensitivity to carbocisteine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Tanta Unuversity

Tanta, Egypt, 31527

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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