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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03358420
Other study ID # HYMC-103-16
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 27, 2017
Last updated November 27, 2017
Start date December 2017
Est. completion date July 2018

Study information

Verified date November 2017
Source Hillel Yaffe Medical Center
Contact Rami Abu Fanne, MD
Phone 972-50-3573694
Email ramia@hadassah.org.il
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to examine the correlation between the severity of non-alcoholic steatohepatitis/non alcoholic fatty liver disease (NASH/NAFLD) in naïve and hepatitis C (HCV) positive patients and the amplitude of alpha-defensin immunohistochemical staining in liver biopsy.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date July 2018
Est. primary completion date July 2018
Accepts healthy volunteers No
Gender All
Age group 15 Years and older
Eligibility Inclusion Criteria:

- Fatty liver disease patients with liver biopsy

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Immunohistochemical staining
Pathological liver slides to be immunohistochemically stained for alpha-defensin

Locations

Country Name City State
Israel Hille Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Amplitude of immunohistochemical stain The amplitude of each slide will be graded from 1-4 Six months
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