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OpenTrials
Completed

NCT Number: NCT00092625

Co-administration Study in Patients With Elevated Cholesterol and Coronary Heart Disease (0653-803)

The purpose of this study is to investigate additional cholesterol lowering effects in patients with coronary heart disease by giving an investigational drug with a patient's current approved cholesterol lowering medication.

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Key information

About this study

The duration of treatment is 10 weeks.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with elevated cholesterol and coronary heart disease

Exclusion criteria

  • Patients who have cholesterol levels within normal ranges as identified by the study

Treatment and study plan

MK0653, ezetimibe

Drug

Comparator: ezetimibe, placebo

Drug

Primary outcomes

  1. Percentage of patients reaching their target LDL-C goal of </= 2.60 mmol/L, after 6 weeks of treatment.

Secondary outcomes

  1. Safety and tolerability.

Sponsors and collaborators

Lead sponsor

Organon and Co

Industry

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate Efficacy, Safety, and Tolerability of Ezetimibe 10 mg or Placebo Added to Existing Atorvastatin 10 mg or 20 mg in Attaining Low-Density Lipoprotein Cholesterol Target Levels in Patients With Hypercholesterolemia and Coronary Heart Disease.

Important dates

Study start
2003
Primary completion
2004
Study completion
2004
First posted
Sep 27, 2004
Registry last updated
Aug 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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