Cholesterol Goal Attainment Rate and Its Associated Factors Among Dyslipidemic Patients on Lipid-lowering Drug Therapy in Korea (CRESENDO)
This study has been completed.
Sponsor:
AstraZeneca
Information provided by (Responsible Party):
AstraZeneca
ClinicalTrials.gov Identifier:
NCT01372956
First received: June 7, 2011
Last updated: December 21, 2011
Last verified: December 2011
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Purpose
This is a multi-centre, cross-sectional, chart review study to investigate cholesterol goal attainment rates defined by modified NCEP-ATP III guidelines and define its possible determinants among Korean dyslipidemic patients
| Condition |
|---|
|
Dyslipidemia |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Only Time Perspective: Retrospective |
| Official Title: | Cholesterol Goal Attainment Rate and Its Associated Factors Among Dyslipidemic Patients on Lipid-lowering Drug Therapy in Korea (CRESCENDO) |
Resource links provided by NLM:
Further study details as provided by AstraZeneca:
Primary Outcome Measures:
- Cholesterol goal attainment rate according to NCEP-ATP III guideline [ Time Frame: Once, at enrollment ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Factors for cholesterol goal achievement: Age, Family history, smoking history, waist circumstance, etc. [ Time Frame: Once, at enrollment ] [ Designated as safety issue: No ]
- Cholesterol goal attainment rate related to CHD or disease history [ Time Frame: Once, at enrollment ] [ Designated as safety issue: No ]
| Enrollment: | 4950 |
| Study Start Date: | August 2011 |
| Study Completion Date: | October 2011 |
| Primary Completion Date: | October 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| Dyslipidemia |
Detailed Description:
MC MD
Eligibility| Ages Eligible for Study: | 19 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
Primary Care
Criteria
Inclusion Criteria:
- Patient who has a dyslipidemia with a lipid profile result within 3 months
- Patient who has a dyslipidemia without change of lipid lowering drug dosage during 3 months after lipid profile test.
Exclusion Criteria:
- Patient who involved in this study previously.
- Patient who participated in other clinical study with study drug within 90 days.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01372956
Locations
| Korea, Republic of | |
| Research Site | |
| Cheongju, Chungcheongbuk-do, Korea, Republic of | |
| Research Site | |
| Cheonan, Chungcheongnam-do, Korea, Republic of | |
| Research Site | |
| Tae, Chungcheongnam-do, Korea, Republic of | |
| Research Site | |
| Anyang, Gyeonggi-do, Korea, Republic of | |
| Research Site | |
| Bucheon, Gyeonggi-do, Korea, Republic of | |
| Research Site | |
| Bundang, Gyeonggi-do, Korea, Republic of | |
| Research Site | |
| Goyang, Gyeonggi-do, Korea, Republic of | |
| Research Site | |
| Guri, Gyeonggi-do, Korea, Republic of | |
| Research Site | |
| Uijeongbu, Gyeonggi-do, Korea, Republic of | |
| Research Site | |
| Gwangju, Jeollabuk-do, Korea, Republic of | |
| Research Site | |
| Iksan, Jeollabuk-do, Korea, Republic of | |
| Research Site | |
| Chuncheon, Kangwon-do, Korea, Republic of | |
| Research Site | |
| Daegu, Kyeongsangbuk-do, Korea, Republic of | |
| Research Site | |
| Deagu, Kyeongsangbuk-do, Korea, Republic of | |
| Research Site | |
| Busan, Kyeongsangnam-do, Korea, Republic of | |
| Research Site | |
| Changwon, Kyeongsangnam-do, Korea, Republic of | |
| Research Site | |
| Busan, Korea, Republic of | |
| Research Site | |
| Gwangju, Korea, Republic of | |
| Research Site | |
| Incheon, Korea, Republic of | |
| Research Site | |
| Seoul, Korea, Republic of | |
Sponsors and Collaborators
AstraZeneca
Investigators
| Principal Investigator: | Jeong Ui Park | Samsung Medical Center |
| Principal Investigator: | Jong sung Kim | Seoul National University Hospital |
| Principal Investigator: | Sung woo Park | Kangbuk Samsung Medical center |
More Information
No publications provided
| Responsible Party: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT01372956 History of Changes |
| Other Study ID Numbers: | NIS-CKR-XXX-2011/1 |
| Study First Received: | June 7, 2011 |
| Last Updated: | December 21, 2011 |
| Health Authority: | South Korea: Korea Food and Drug Administration (KFDA) |
Keywords provided by AstraZeneca:
|
LDL-C, cholesterol, risk factor |
Additional relevant MeSH terms:
|
Dyslipidemias Lipid Metabolism Disorders Metabolic Diseases Hypolipidemic Agents Antimetabolites |
Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Lipid Regulating Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 21, 2013