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NCT00526552 Clinical Trial

Crestor RAPID (The Efficacy of RosuvAstatin for Korean Dyslipidemia PatIents With Diabetes)

Diabetes Clinical Trial

— RAPID  

Official title:
RAPID (Evaluating the Efficacy of RosuvAstatin for Korean Dyslipidemia PatIents With Diabetes in Real World Practice)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00526552
Other study ID # NIS-CKR-CRE-2007/3
Secondary ID
Status Completed
Phase N/A
First received September 5, 2007
Last updated March 29, 2010
Start date June 2007
Est. completion date December 2007

Study information
Verified date March 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Observational

Clinical Trial Summary

To evaluate the efficacy of rosuvastatin in Korean dyslipidemia patients with diabetes

Recruitment information / eligibility
Status Completed
Enrollment 5000
Est. completion date December 2007
Est. primary completion date August 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Hyperlipidemia patients who are prescribed with rosuvastatin 10mg, based on clinical grounds and fulfil the following criteria

1. Over 18 years of age

2. Diagnosed with DM based on fasting or post-load glucose data and/or clinical assessment by the clinician

Exclusion Criteria:

1. Patients already taking other hyperlipidemic agents

2. Patients who do not fulfil the indication criteria for statin therapy

3. Patients who do not have baseline and/or follow-up lipid data to verify the efficacy data

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Korea, Republic of Research Site Seoul Jongro-gu
Korea, Republic of Research Site Seoul Kangnam-gu
Korea, Republic of Research Site Seoul Songpa-gu

Sponsors (1)
Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Korea, Republic of, 

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