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A 12 Week Study to Assess the Effectiveness of an Investigational Cholesterol-Lowering Drug in Patients That Have Been Hospitalized for a Possible Heart Problem - Article


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Cholesterol


Clinical Trial: A 12 Week Study to Assess the Effectiveness of an Investigational Cholesterol-Lowering Drug in Patients That Have Been Hospitalized for a Possible Heart Problem

This study is currently recruiting patients.
Verified by Merck July 2005

Sponsored by: Merck
Information provided by: Merck
ClinicalTrials.gov Identifier: NCT00132717

Purpose

Investigate the effect of an investigational cholesterol-lowering drug in patients who are currently taking an approved medication for hypercholesterolemia (high cholesterol levels) and have been hospitalized for a heart problem.

(INTERNATIONAL STUDY LOCATIONS ONLY)

Condition Intervention Phase
Hypercholesterolemia
 Drug: MK0653A, ezetimibe (+) simvastatin
Phase IV

MedlinePlus related topics:  Cholesterol

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • Patients greater than 18 years old, who were admitted to a hospital for an investigation of a heart problem and currently receiving an approved medication to lower cholesterol

Exclusion Criteria:

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00132717


Australia
      Merck Sharp & Dohme (Australia) Pty Ltd., South Granville,  NSW 2142,  Australia; Recruiting
Linda Swan, MD  612-9795-9377 

Austria
      Merck Sharp & Dohme Gmbh, Vienna,  1220,  Austria; Recruiting
Andras Madai, MD  43.1.26.044.182 

Belgium
      Merck Sharp & Dohme B.V., BRUXELLES,  1180,  Belgium; Recruiting
Dirk Poelaert, MD  32-2-373-4310 

Chile
      Merck Sharp & Dohme (I.A.) Corp., Santiago,  6761641,  Chile; Recruiting
Margarita Charlin, MD  562-655-8850 

Croatia
      Merck Sharp & Dohme IDEA, Inc., Zagreb,  10 010,  Croatia; Recruiting
Goranka Glad Scherr, MD  385 1 66 44 336 

France
      Laboratoires Merck Sharp & Dohme - Chibret, Paris Cedex 8,  75114,  France; Recruiting
Jean-Marie Goehrs, MD  (33.1) 47.54.89.90 

Germany
      Msd Sharp & Dohme Gmbh, Haar,  85540,  Germany; Recruiting
Ottfried Zierenberg, PhD  49 89 4561 1102 

Hong Kong, Hong Kong Island
      Merck Sharp & Dohme (Asia) Ltd., Causeway Bay,  Hong Kong Island,  Hong Kong; Recruiting
Linda Semlitz (Gilbert), MD  852 2835-9860 

Italy
      Merck Sharp & Dohme (Italia) S.P.A., Roma,  191,  Italy; Recruiting
Gianfranco Botta, MD  +39 06 36 191 187 

Malaysia
      Merck Sharp & Dohme (I.A.) Corp, Selangor,  46300,  Malaysia; Recruiting
Nazrin Azli, MD  603-79662848 

Singapore
      Merck Sharp & Dohme (Singapore), Singapore,  199555,  Singapore; Recruiting
Justin Chin, MD  +65 6393 7683 

Switzerland
      Merck Sharp & Dohme - Chibret, A.G., Glattbrugg,  8152,  Switzerland; Recruiting
Martin Fenner, MD  0041-1-828 7308 

United Kingdom, Hertfordshire
      Merck Sharp & Dohme Ltd., Hoddesdon,  Hertfordshire,  EN11 9BU,  United Kingdom; Recruiting
John Young, MD  44 1992 452341 

Study chairs or principal investigators

Medical Monitor,  Study Director,  Merck   

More Information

Study ID Numbers:  2004_046
Last Updated:  August 19, 2005
Record first received:  August 2, 2005
ClinicalTrials.gov Identifier:  NCT00132717
Health Authority: France: Afssaps - French Health Products Safety Agency
ClinicalTrials.gov processed this record on 2005-08-23


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