Clinical Trials Directory

Trials / Completed

CompletedNCT07313124

Comparative Study Between Antihyperlipidemic Agents in Treatment of Cardiovascular Diseases

The Efficiency and Safety of Single Drug Versus Combinations of Antihyperlipidemic Agents in Treatment of Cardiovascular Diseases

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Beni-Suef University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to study the efficiency and safety of using combinations of antihyperlipidemic agents with a single drug to treat cardiovascular diseases. The main questions it aims to answer are: * Which approach is more effective rosuvastatin monotherapy or rosuvastatin ezetimibe combination antihyperlipidemic for patients with cardiovascular diseases (CVDs)? * What medical problems do participants could when taking antihyperlipidemic drugs? Researchers will compare rosuvastatin 20 mg or rosuvastatin ezetimibe10/10mg to see the effectiveness and safety of these drugs in patients with CVDs. Participants will: * Patients will randomize to either rosuvastatin 20 mg or rosuvastatin ezetimibe10/10mg. * Patients will be followed up to 12 weeks after starting treatment. * All the patients will be subjected to: Full sheet taking, including detailed history and diagnosis of the case, Baseline Aspartate aminotransferase (AST) and Alanine Aminotransferase (ALT) tests\& after 24 weeks of treatment, Lipid Profile, creatine kinase (CK) test, Creatine kinase-MB (CK-MB) test.

Conditions

Interventions

TypeNameDescription
DRUGrosuvastatin drugPatients randomized to receive rosuvastatin 20 mg
COMBINATION_PRODUCTPatients received rosuvastatin ezetimibe10/10mgPatients received rosuvastatin ezetimibe10/10mg

Timeline

Start date
2024-12-15
Primary completion
2025-11-20
Completion
2025-12-01
First posted
2025-12-31
Last updated
2026-01-05

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07313124. Inclusion in this directory is not an endorsement.