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

This study has been completed.
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ClinicalTrials.gov Identifier:
First received: October 5, 2005
Last updated: November 18, 2010
Last verified: November 2010
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 Phase
Diabetes Mellitus Type 2
Crestor, Rosuvastatin
LDL Cholesterol
Phase 4

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: DIALOOG: Crestor in Patients With Diabetes Mellitus Type 2: Lowering of LDL-C Levels to New European Guidelines

Resource links provided by NLM:

Further study details as provided by AstraZeneca:

Estimated Enrollment: 2500
Study Start Date: May 2004

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Diabetes Mellitus Type 2

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
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00233649

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Sponsors and Collaborators
Study Director: Astra Zeneca AstraZeneca
  More Information

ClinicalTrials.gov Identifier: NCT00233649     History of Changes
Other Study ID Numbers: NL401017 
Study First Received: October 5, 2005
Last Updated: November 18, 2010
Health Authority: European Union: European Medicines Agency

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Endocrine System Diseases
Glucose Metabolism Disorders
Metabolic Diseases

ClinicalTrials.gov processed this record on May 23, 2016