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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00687492
Other study ID # NIS-CAP-DUM-2008/1
Secondary ID
Status Completed
Phase N/A
First received May 28, 2008
Last updated December 1, 2010
Start date May 2008
Est. completion date December 2008

Study information

Verified date December 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Philippines: Bureau of Food and Drugs
Study type Observational

Clinical Trial Summary

The survey will try to establish the proportion of patients on lipid-lowering pharmacological treatment reaching the LDL-C goals according to the third NCEP ATP guidelines, overall and by country.


Recruitment information / eligibility

Status Completed
Enrollment 8000
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 2 or more risk factors (according to NCEP ATP III guideline)

- Receiving lipid-lowering drug treatment for at least 3 months without dosage change for a minimum of 6 weeks.

Exclusion Criteria:

- Involvement in the planning and conduct of the study (applies to both AstraZeneca staff or staff at the study site).

- Previous enrolment or randomisation of treatment in the present study.

- Participation in a clinical study during the last 90 days.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Research Site Hong Kong Hong Kong
Indonesia Research Site Bandung West Java
Indonesia Research Site Jakarta DKI Jakarta
Indonesia Research Site Medan North Sumatra
Indonesia Research Site Semarang Central Java
Indonesia Research Site Sidoarjo East Java
Indonesia Research Site Surabaya East Java
Korea, Republic of Research Site Bu-cheon Gyeong-gi
Korea, Republic of Research Site Bu-san
Korea, Republic of Research Site Bundang Gyeong-gi
Korea, Republic of Research Site Cheon-an Chung-Cheong-nam-do
Korea, Republic of Research Site Dae-gu
Korea, Republic of Research Site Dae-jeon
Korea, Republic of Research Site Gu-ri Gyeong-gi
Korea, Republic of Research Site Gwangju
Korea, Republic of Research Site Il-san Gyeong-gi
Korea, Republic of Research Site In-cheon
Korea, Republic of Research Site Je-ju
Korea, Republic of Research Site Ma-san Gyung-sang-nam-do
Korea, Republic of Research Site Seoul
Korea, Republic of Research Site Su-won Gyeong-gi
Korea, Republic of Research Site Ul-san
Malaysia Research Site Ampang Selangor
Malaysia Research Site Bandar Sunway Selangor
Malaysia Research Site Bangsar Kuala Lumpur
Malaysia Research Site Batu Caves Selangor
Malaysia Research Site Hulu Selangor Selangor
Malaysia Research Site Kepong Kuala Lumpur
Malaysia Research Site Klang Selangor
Malaysia Research Site Kuala Lumpur
Malaysia Research Site Petaling Jaya Selangor
Malaysia Research Site Port Klang Selangor
Malaysia Research Site Puchong Kuala Lumpur
Malaysia Research Site Sekinchan Selangor
Malaysia Research Site Selangor
Malaysia Research Site Seri Kembangan Selangor
Malaysia Research Site Setapak Kuala Lumpur
Malaysia Research Site Shah Alam Selangor
Malaysia Research Site Subang Selangor
Malaysia Research Site Subang Jaya Selangor
Malaysia Research Site Sungai Buloh Selangor
Philippines Research Site Baguio Benguet
Philippines Research Site Davao
Philippines Research Site Iloilo
Philippines Research Site Lipa Batangas
Philippines Research Site Manila
Taiwan Research Site Kaohsiung
Taiwan Research Site Taichung
Taiwan Research Site Tainan
Taiwan Research Site Taipei
Taiwan Research Site Taoyuan
Thailand Research Site Bangkoknoi Bangkok
Thailand Research Site Dusit Bangkok
Thailand Research Site Klongluang Pathumthani
Thailand Research Site Muang ChiangMai
Thailand Research Site Pathumwan Bangkok
Thailand Research Site Ratchathewi Bangkok
Vietnam Research Site Hanoi
Vietnam Research Site Hcmc

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Countries where clinical trial is conducted

China,  Indonesia,  Korea, Republic of,  Malaysia,  Philippines,  Taiwan,  Thailand,  Vietnam, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number and percentage of subjects achieving the LDL-C goals according to updated 2004 NCEP ATP ? guidelines(overall and by country) After collecting all Patient Record Form. No
Secondary The number and percentage of subjects achieving the LDL-C goals according to the updated 2004 NCEP ATP ? guidelines for several subject subsets. After collecting all Patient Record Form. No
Secondary The association between achievement of LDL-C goals,according to the updated 2004 NCEP ATP? guidelines and patient and physician variables. After collecting all Patient Record Form. No
Secondary The physician characteristics associated with the allocation of hypercholesterolemia treatment regime. After collecting all Patient Record Form. No
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