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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06445335
Other study ID # CTU2019009
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 1, 2019
Est. completion date November 1, 2024

Study information

Verified date May 2024
Source Ziekenhuis Oost-Limburg
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine the prevalence of non-alcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes mellitus (T2DM).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 385
Est. completion date November 1, 2024
Est. primary completion date November 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - = 18 years of age - Having type 2 diabetes mellitus (T2DM) - Written informed consent obtained Exclusion Criteria: - Excessive alcohol use - Exclusion of other causes of liver disease and secondary causes of steatosis

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
FibroScan
Performance of a FibroScan measurement.

Locations

Country Name City State
Belgium Ziekenhuis Oost-Limburg Genk Limburg

Sponsors (1)

Lead Sponsor Collaborator
Ziekenhuis Oost-Limburg

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of non-alcoholic fatty liver disease (NAFLD) in type 2 diabetes mellitus (T2DM) patients To determine the prevalence of non-alcoholic fatty liver disease (NAFLD) in type 2 diabetes mellitus (T2DM) patients followed at the department of Endocrinology in Ziekenhuis Oost-Limburg (ZOL), Genk, Belgium by means of FibroScan measurements. Baseline
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