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Clinical Trials/NCT06445361
NCT06445361RecruitingNot Applicable

The Prevalence of Non-Alcoholic Fatty Liver Disease in Type 1 Diabetes Mellitus Patients Followed at Ziekenhuis Oost-Limburg, Genk, Belgium

Ziekenhuis Oost-Limburg2 sites in 1 country138 target enrollmentStarted: July 1, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
138
Locations
2
Primary Endpoint
Prevalence of fibrosis in T1DM

Study Overview

Brief Summary

To determine the prevalence of NAFLD in T1DM patients.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • ≥ 18 years of age
  • Written informed consent obtained

Exclusion Criteria

  • Excessive alcohol use
  • Exclusion of other causes of liver disease and secondary causes of liver steatosis

Outcomes

Primary Outcomes

Prevalence of fibrosis in T1DM

Time Frame: During the intervention

To determine the prevalence of fibrosis in a cohort of T1DM patients followed at the Departments of Endocrinology in ZOL by means of the FibroScan® device with vibration controlled attenuation parameter (VCTE) measurements.

Prevalence of NAFLD in T1DM

Time Frame: During the intervention

To determine the prevalence of steatosis in a cohort of T1DM patients followed at the Departments of Endocrinology in ZOL by means of the FibroScan® device with controlled attenuation parameter (CAP) measurements.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Ziekenhuis Oost-Limburg
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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