Medical Students' Evaluation of Dyslipidemia and LIPoprotein(a) Study
NCT ID: NCT06482476
Last Updated: 2024-07-01
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.
RECRUITING
246 participants
OBSERVATIONAL
2024-06-30
2024-10-31
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.
The Hellenic Postprandial Lipemia Study (HPLS)
NCT02163044
A Study to Evaluate Fasting/Postprandial Serum Apolipoprotein B-48 (ApoB-48) Levels in Diabetic Participants With Normal to Moderately High Low Density Lipoprotein-C (LDL-C) Levels (MK-0653A-259 AM1)
NCT01333436
Effects of a Digital Health Application (Lipodia) on LDL-cholesterol Levels
NCT05988866
Effect of Mediterranean Diet in Dyslipidemic Patients
NCT04486664
The Effect of Childhood Dyslipidemia on Endothelial and Renal Function
NCT03856476
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.
ECOLOGIC_OR_COMMUNITY
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Med students
Medical students in whom Lp(a) levels will be measured
Measurement of Lp(a) levels
Collection of a venous blood sample for the measurement of Lp(a) levels using standardized laboratory methods
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Measurement of Lp(a) levels
Collection of a venous blood sample for the measurement of Lp(a) levels using standardized laboratory methods
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Ioannina
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Fotios Barkas
Fotios Barkas, MD, MSc, PhD, Assistant Professor of Internal Medicine Faculty of Medicine, School of Health Sciences, University of Ioannina, Ioannina, Greece
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Fotios Barkas, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Ioannina
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Hospital of Ioannina
Ioannina, Ioannina, Greece
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.
MEDLIP Study
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.