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Effect of Ezetimibe on Oxidized Low-density Lipoprotein (LDL) Cholesterol

Effect of Ezetimibe on Oxidized LDL Cholesterol

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01008345
Enrollment
100
Registered
2009-11-05
Start date
2008-09-30
Completion date
2009-06-30
Last updated
2009-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Diabetes

Brief summary

Randomized study. Patients with coronary artery disease equivalent will be randomized to receive atorvastatin 40 mg/day + placebo vs. atorvastatin 40 mg/day + ezetimibe 40 mg/day. Oxidized LDL cholesterol will be measured at baseline and after 8 weeks of treatment. Hypothesis is that ezetimibe will lower oxidized LDL

Interventions

DRUGezetimibe

Patients will receive 10 mg/day of ezetimibe for 8 weeks

Sponsors

Pharmaline, Lebanon
CollaboratorUNKNOWN
Hotel Dieu de France Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* CAD or CAD equivalent

Exclusion criteria

* Prior CABG or PCI within 3 months Prior use of ezetimibe within 3 months Receiving atorvastatin 40 mg/day or 80 mg/day or any dose of rosuvastatin CHF NYHA stage \>2 Creatinin clearance \< 30 ml/min

Design outcomes

Primary

MeasureTime frame
level of oxidized LDL cholesterol at end of study8 weeks of treatment

Secondary

MeasureTime frame
small dense LDL level8 weeks of treatment

Countries

Lebanon

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026