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CompletedNCT00526552RAPIDUpdated Mar 30, 2010

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

An observational study in Dyslipidemia and Diabetes, sponsored by AstraZeneca. Completed at 3 sites in Korea, Republic of. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-03-30.

Sponsored by AstraZeneca · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
5,000
Ages
18 Years and older
Sex
All
01

Study summary

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

02

Conditions studied

  • Dyslipidemia
  • Diabetes

Keywords

  • dyslipidemia
  • rosuvastatin
  • diabetes
  • cholesterol
  • Naturalistic
  • Observational
03

In context

Diabetes Mellitus

10,923 studies on the registry are indexed under Diabetes Mellitus; 1,318 are open to participants now.

This study's planned enrollment of 5,000 is above the median of 233 across 2,218 observational studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

AstraZeneca is the lead sponsor of 3,429 studies on the registry; 270 are open to participants now.

Of its 357 completed or terminated interventional studies of FDA-regulated products, 173 (48%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Diabetic Mellitus patients with hypercholesteromia in Korean tertiary care centers

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

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
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
5,000 participants (estimated)
06

Study locations

3 sites
  • Research Site
    Seoul, Jongro-gu, Korea, Republic of
  • Research Site
    Seoul, Kangnam-gu, Korea, Republic of
  • Research Site
    Seoul, Songpa-gu, Korea, Republic of
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00526552
Lead sponsor
AstraZeneca
First posted
Sep 10, 2007
Start date
Jun 2007
Primary completion
Aug 2007
Completion
Dec 2007
Last update
Mar 30, 2010

Study contacts

Hyunah Caroline Choi
study director · AstraZeneca Korea

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2010. You cannot join it, but the record below documents what was studied.

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