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Clinical Trial Summary

This study included 70 subjects divided into 3 groups. Group I included 25 patients with NAFLD. Group II included 25 patients with NAFLD and chronic HCV. Group III: included 20 controls. Abdominal ultrasound was done to patients and controls. Plasma pentraxin-3 (PTX3) was measured using ELISA. Comparison between three groups was done regarding plasma pentraxin-3. Higher levels of plasma PTX3 were detected in NAFLD patients irrespective of presence or absence of chronic HCV infection. Plasma PTX3 could be used as a non-invasive test for prediction of metabolic syndrome in the high-risk population with high sensitivity and moderate specificity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03276039
Study type Observational
Source Ain Shams University
Contact
Status Completed
Phase N/A
Start date April 15, 2014
Completion date July 30, 2016

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