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Effect of Treatment With Insulin Sensitizer on Arterial Properties, Metabolic Parameters and Liver Function in Patients With Nonalcoholic Fatty Liver Disease

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01084486
Enrollment
Unknown
Registered
2010-03-10
Start date
Unknown
Completion date
Unknown
Last updated
2010-03-10

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

Conditions

Nonalcoholic Fatty Liver Disease

Keywords

nonalcoholic fatty liver disease, Pulse wave velocity, augmentation index, metformin

Brief summary

Abstract Background: Insulin resistance has an important role in the development of nonalcoholic fatty liver disease (NAFLD) and is involved in both pathological processes: hepatic steatosis and atherosclerosis. Therefore, treatment of NAFLD with insulin sensitizers is likely to have a favorable effect towards hepatic steatosis and cardiovascular outcomes. Objectives: The present study investigated the effect of metformin on arterial properties, metabolic parameters and liver function in patients with NAFLD. Methods In randomized, placebo controlled study, 63 patients with NAFLD were assigned to one of two groups: Group 1 received daily metformin; Group 2 received placebo. Pulse wave velocity (PWV) and augmentation index (AI) were performed using SphygmoCor (version 7.1, AtCor Medical, Sydney, Australia) at baseline and at the end of 4-month treatment period.. Metabolic measures and serum adiponectin levels were determined.

Interventions

DRUGMetformin

Sponsors

Wolfson Medical Center
Lead SponsorOTHER_GOV

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* In a single-center study, 63 patients (32 males and 31 females) diagnosed with nonalcoholic fatty liver disease were recruited from the outpatient clinic and evaluated for the study.

Exclusion criteria

* Patients with history of unstable angina, MI, CVA or major surgery within the six months preceding entrance to the study. * Patients with unbalanced endocrine disease or any disease that might affect absorption of medications. * Patients with plasma creatinine \> 1.5 mg/dl, and electrolyte abnormalities.

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 16, 2026