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CompletedNCT00651560

Vytorin As Strategy To Reduce Dislipidemia In Adults (0653A-148)

Vytorin As Strategy To Reduce Dislipidemia In Adults

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
167 (actual)
Sponsor
Organon and Co · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is intended to allow physicians to check the superior clinical efficacy of Vytorin compared to atorvastatin, as the most adequate therapy using the ATP-III goals achievement and cardiovascular risk reduction in adult patients with dislipidemia.

Conditions

Interventions

TypeNameDescription
DRUGezetimibe (+) simvastatinezetimibe 10mg (+) simvastatin 20 mg once daily for 4 weeks of treatment.

Timeline

Start date
2005-11-01
Primary completion
2005-12-23
Completion
2005-12-23
First posted
2008-04-03
Last updated
2024-08-15

Source: ClinicalTrials.gov record NCT00651560. Inclusion in this directory is not an endorsement.

Vytorin As Strategy To Reduce Dislipidemia In Adults (0653A-148) (NCT00651560) · Clinical Trials Directory