Clinical Trials Directory

Trials / Completed

CompletedNCT05284448

Pentoxifylline in Treatment of Patients With Nonalcoholic Steatohepatitis

Effectiveness and Safety of Pentoxifylline in Treatment of Patients With Nonalcoholic Steatohepatitis

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Al-Azhar University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The aim of the present study is to evaluate the efficacy and safety of pentoxifylline in the treatment of non-alcoholic steatohepatitis patients.

Detailed description

Nonalcoholic steatohepatitis(NASH) is the progressive form of Non-alcoholic fatty liver disease (NAFLD), is characterized by hepatocellular damage, inflammation, and liver fibrosis that can progress to cirrhosis, in 25% of patients, NAFLD progresses to NASH, which increases the risk for the development of cirrhosis, liver failure, and hepatocellular carcinoma. In patients with NASH, liver fibrosis is the main determinant of mortality. Pentoxifylline (PTX) is a xanthine derivative drug with a wide range of actions at the cellular and molecular level. PTX possess anti-inflammatory, antioxidant activities. PTX have potential role in improvement of NASH . Also, PTX inhibits a number of pro-inflammatory cytokines including interleukin-1, interleukin-6 and tumor necrosis factor (TNF-α ) which play an important role in the pathogenesis and progression of NASH.

Conditions

Interventions

TypeNameDescription
DRUGpentoxifylline (Trental SR®)400 mg three times daily

Timeline

Start date
2022-02-01
Primary completion
2022-09-01
Completion
2022-10-01
First posted
2022-03-17
Last updated
2024-06-21

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05284448. Inclusion in this directory is not an endorsement.