DIALOOG: Crestor in Patients With Diabetes Mellitus Type 2: Lowering of LDL-C Levels to New European Guidelines

Sponsor
AstraZeneca (Industry)
Overall Status
Completed
CT.gov ID
NCT00233649
Collaborator
(none)
2,500
222
11.3

Study Details

Study Description

Brief Summary

The purpose of this study is to determine in DM II patients the efficacy of Crestor in obtaining the new European LDL cholesterol guidelines.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Time Perspective:
    Prospective
    Official Title:
    DIALOOG: Crestor in Patients With Diabetes Mellitus Type 2: Lowering of LDL-C Levels to New European Guidelines
    Study Start Date :
    May 1, 2004

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 70 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • Diabetes Mellitus Type 2, LDL-C > 2,5 mmol/l, no cholesterol lowering medication used last 3 months, starts with Crestor 10 mg, permission to use patient data by AZ

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      Locations

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      Sponsors and Collaborators

      • AstraZeneca

      Investigators

      • Study Director: Astra Zeneca, AstraZeneca

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00233649
      Other Study ID Numbers:
      • NL401017
      First Posted:
      Oct 6, 2005
      Last Update Posted:
      Nov 19, 2010
      Last Verified:
      Nov 1, 2010
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Nov 19, 2010