PADAC: Prevalence of NAFLD in ACS Patients

Sponsor
Hasselt University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05378321
Collaborator
(none)
1,000
1
1
49.9
20

Study Details

Study Description

Brief Summary

Addressing CVD risk in patients with NAFLD is the aspect of the disease most amenable to medical management and so improving long-term clinical outcomes. Almost no studies have been done concerning the prevalence of NAFLD in CVD patients, most of the conducted studies have been done in already diagnosed NAFLD patients to estimate the risk of CVD development. Currently, there are no data available about the prevalence of NAFLD in CVD, more specifically patients with an acute cardiovascular event (ACE) in Belgium.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Non-invasive diagnostic testing
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1000 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
The Prevalence of Non-Alcoholic Fatty Liver Disease in Patients With an Acute Cardiac Event Followed at Ziekenhuis Oost-Limburg, Genk, Belgium
Actual Study Start Date :
Feb 1, 2022
Anticipated Primary Completion Date :
Apr 1, 2026
Anticipated Study Completion Date :
Apr 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Other: ACS risk gropu

Group of patients with an acute-cardiovascular syndrome.

Diagnostic Test: Non-invasive diagnostic testing
Non-invasive diagnostic testing consists of the use of the FibroScan device and the calculation of non-invasive blood-based scores for the diagnosis of NAFLD

Outcome Measures

Primary Outcome Measures

  1. FibroScan® liver stiffness measurements [4 years]

    The FibroScan® device measures vibration controlled transient elastography (VCTE) (kPa) Based on these values the liver stiffness status will be determined.

  2. FibroScan® steatosis measurements [4 years]

    The FibroScan® device measures controlled attenuation parameter (CAP) (dB/m) Based on these values the liver steatosis status will be determined.

  3. Liver ultrasound [4 years]

    Out of the EPF the results of a possible earlier ultrasound are noted in the CRF. The results are noted as 'liver steatosis found' with yes/no answer and the year in which this ultrasound was performed.

  4. Liver biopsy results [4 years]

    Out of the EPF the results of a possible earlier ultrasound or liver biopsy are noted in the CRF. The NAS CRN (histological) score is noted. The score ranges from 0-8 and is composed of the unweighted sum of steatosis, ballooning, and lobular inflammation. A score between 0-2 corresponds to no NASH, 3-4 is borderline NASH, and definite NASH has a score between 5 and 8.

  5. Aspartate transaminase (AST) [4 years]

    Out of the EPF the blood parameter AST (U/L) will be collected.

  6. Alanine transaminase (ALT) [4 years]

    Out of the EPF the blood parameter ALT (U/L) will be collected.

  7. Gamma glutamyltransferase (GGT) [4 years]

    Out of the EPF the blood parameter GGT (U/L) will be collected.

  8. Lactate dehydrogenase (LDH) [4 years]

    Out of the EPF the blood parameter LDH (U/L) will be collected.

  9. Exclusion of other liver diseases [4 years]

    hepatitis B, hepatitis C, autoimmune hepatitis, primary biliary cirrhosis, hemochromatosis, Wilson disease and alpha 1 antitrypsin deficiency. NAFLD is a disease of exclusion and therefore the abovementioned parameters are determined out of the EPF.

  10. Wellbeing - BAECKE [4 years]

    This questionnaire will be used to estimate the level of physical activity. It exists out of 16 questions about work, sports and leisure time. A higher score means that the person is more active at work, does more sport and has a more active leisure time. Minimum value is 3 and maximum value is 15.

  11. Wellbeing - GAD-7 [4 years]

    General Anxiety Disorder (GAD-7) questionnaire will be used to determine the presence of possible clinically significant anxiety disorder. A higher scores indicates having anxiety. Minimum score is 0 and maximum score is 21.

  12. Wellbeing - PHQ-9 [4 years]

    Patient Health Questionnaire-9 (PHQ-9) will be used to quantify depression symptoms and monitor severity. Minimum score is 0 and maximum score is 27. A higher score indicates having a depression.

  13. Wellbeing - WPAI-SHP [4 years]

    Workers Productivity and Activity Impairment (WPAI-SHP) questionnaire. By means of 6 questions about work productivity and activity it can be determined if there is absence, productivity loss or a decrease in activities at work. The score is expressed in percentages (0-100). A higher percentage indicates a higher absence from work and a lower productivity.

  14. Wellbeing-SF-36 [4 years]

    Short Form Health Survey-36 will be used to determine the health related quality of life based on 6 different topics: physical functioning, social functioning, role restrictions, mental wellbeing, energy and pain. The score is expressed in percentages (0-100). A higher percentage indicates a better general wellbeing.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 years

  • having acute cardiovascular syndrome

  • able to understand Dutch

  • able to understand the informed consent

Exclusion Criteria:
  • excessive alcohol abuse

  • other liver disease

  • secondary causes of steatosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ziekenhuis Oost-Limburg Genk Limburg Belgium 3600

Sponsors and Collaborators

  • Hasselt University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Geert Robaeys, Prof. Dr. Geert Robaeys, Hasselt University
ClinicalTrials.gov Identifier:
NCT05378321
Other Study ID Numbers:
  • PADAC-01
First Posted:
May 18, 2022
Last Update Posted:
May 18, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 18, 2022