Subclinical Cardiovascular Changes in NAFLD Patient (Predictive Value of Speckle Tracking Echocardiography )
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ClinicalTrials.gov Identifier: NCT05790057 |
Recruitment Status :
Not yet recruiting
First Posted : March 29, 2023
Last Update Posted : March 29, 2023
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the goal of this study (observational study ) is to learn about the subclinical cardiovascular changes in patients with nonalcoholic fatty liver . the main questions it aims to answer are
- the role of speckle tracking echocardiogram in detection of subclinical cardiovascular complication in NAFLD patients
- the role of fibroscan in diagnosis of nonalcoholic fatty liver the participant will be examined by fibroscan and speckle tracking echocardiogram
Condition or disease |
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Liver Steatoses |

Study Type : | Observational |
Estimated Enrollment : | 60 participants |
Observational Model: | Other |
Time Perspective: | Cross-Sectional |
Official Title: | Subclinical Cardiovascular Changes in Patient With Non Alcoholic Fatty Liver Disease (Predictive Value of Speckle Tracking Echocardiography ) |
Estimated Study Start Date : | May 1, 2023 |
Estimated Primary Completion Date : | March 1, 2025 |
Estimated Study Completion Date : | October 1, 2025 |

- the sensitivity of fibroscan in diagnosis of NAFLD [ Time Frame: baseline ]analysis of the results of fibroscan and test the sensitivity of fibroscan in measurement the degree of steatosis and diagnosis of NAFLD
- role of speckle tracking echocardiogram in detection of subclinical cardiovascular complications of NAFLD [ Time Frame: baseline ]speckle tracking echocardiogram will be used to to find any cardiac abnormality such as myocardial infarction , valvular diseases in NAFLD patients
- comparison between conventional echocardiogram and speckle tracking echocardiogram in detection of subclinical cardiovascular complications of NAFLD patients [ Time Frame: baseline ]comparison between the results and measurements of both conventional echocardiogram and speckle tracking echocardiogram

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Patients above age of 18 years old
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All patients showing degree of fibrosis and steatosis
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Exclusion Criteria:
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1-Patients diagnosed with cardiac disease (previous or current )
2-patients known to have chronic liver disease
3-patients younger than 18 years old
4-patients with hepatocellular cancer
5-patients know to be alcoholic
6-patients with previous history of hypertension

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05790057
Contact: omar m magdy, postgraduate | 01062983336 ext 02 | omar.megooz96@gmail.com | |
Contact: reem e mahdy, PHD | 01096608866 ext 02 | reemezzat@gmail.com |
Egypt | |
Assiut university | |
Assiut, Assuit, Egypt, 71515 | |
Contact: reem e mahdy, professor 01096608866 ext 02 reemezzat1@gmail.com |
Study Director: | lobna m abdelwaheed, professor | supervisor of the research ( professor of internal medicine Assiut university | |
Study Director: | soheir m kasem, professor | supervisor of the research ( professor of internal medicine Assiut university |
Responsible Party: | Omar Mohamed Magdy Eid, pricipal investigator , internal medicine resident, Assiut University |
ClinicalTrials.gov Identifier: | NCT05790057 |
Other Study ID Numbers: |
cardiac complication in NAFLD |
First Posted: | March 29, 2023 Key Record Dates |
Last Update Posted: | March 29, 2023 |
Last Verified: | March 2023 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Fatty Liver Liver Diseases Digestive System Diseases |