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N-acetyl Cysteine and Patients with Non-alcoholic Fatty Liver Disease

A

Ain Shams University

Status and phase

Completed
Phase 3

Conditions

Simple Steatosis Non Fatty Liver

Treatments

Drug: N acetyl cysteine with weight reduction

Study type

Interventional

Funder types

Other

Identifiers

NCT05589584
1234867

Details and patient eligibility

About

Effect of N-acetyl cysteine on markers of oxidative stress and insulin resistance in patients with Non-alcoholic fatty liver disease

Enrollment

60 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males or females aged 18-60 years diagnosed with NAFLD

Exclusion criteria

  • History of alcohol consumption, drug addiction or the use of medications known to precipitate steatohepatitis.
  • Patients with schistosomiasis, active hepatitis B or C, autoimmune and diabetes mellitus.
  • current Consumption of any antioxidant supplements and hepatotoxic drug.
  • Pregnancy or lactation or expecting to get pregnant during the study.
  • Medical, psychological, or pharmacological factors interfering with the collection or interpretation of study data.
  • Active Cancer patients.
  • Anyone having hypersensitivity to N-acetylcysteine.
  • Anyone already taking N-acetylcysteine.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

intervention
Experimental group
Description:
NAC and weight reduction program
Treatment:
Drug: N acetyl cysteine with weight reduction
control
No Intervention group
Description:
weight reduction program only

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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