Epicardial Fat, Visceral Fat and Coronary Atherosclerosis
NCT ID: NCT01344694
Last Updated: 2011-05-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
110 participants
OBSERVATIONAL
2011-07-31
2012-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Visceral Abdominal Fat, Non Alcoholic Fatty Liver Diseases and Asymptomatic Coronary Atherosclerosis
NCT01282892
Visceral Adiposity and CVD Risk in Women
NCT00021879
Abdominal Fat and Imaging Measurements of Heart Disease
NCT01447745
Visceral Fat, Metabolic Rate, and CHD Risk in Young Adults
NCT00005388
The Weight of Cardiovascular Disease
NCT06053645
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
patient with liver fat
30 patients with liver fat
patient with liver fat
30 patient with liver fat
excess of visceral fat
50 pts. with excess of visceral fat
pts. with excess of visceral fat
pts. with excess of visceral fat
control
30 control subjects
control
30 control subjects
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
patient with liver fat
30 patient with liver fat
pts. with excess of visceral fat
pts. with excess of visceral fat
control
30 control subjects
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* patients with excess of visceral fat,
* 30 patients with liver fat accumulation
* 30 sex-age-matched individual (controls) will be enrolled. All patients will undergo a complete family history, personal clinical history, physical examination and blood sampling for biochemical analysis.
* Informed consent will be obtained from each individual.
Exclusion Criteria
* recent history of acute illness,
* clinical history of ischemic heart disease and cerebrovascular disease,
* typical chest pain,
* previous coronary artery disease,
* conventional coronary angiography, percutaneous interventions, coronary by pass grafting, renal failure, cancer patients,
* subjects who take drugs that induces hepatic steatosis ( corticosteroids, estrogens, methotrexate, amiodarone and others)
40 Years
70 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ziv Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ziv Medical center
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nimer Assy, md
Role: PRINCIPAL_INVESTIGATOR
Ziv MC
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ziv MC
Safed, , Israel
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
0020-11
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.