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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00684151
Other study ID # NIS-CTH-DUM-2007/1
Secondary ID
Status Completed
Phase N/A
First received May 22, 2008
Last updated December 9, 2011
Start date April 2008
Est. completion date November 2011

Study information

Verified date December 2011
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Thailand: Ministry of Public Health
Study type Observational

Clinical Trial Summary

The first phase of the study is a hospital-based cross-sectional, epidemiological survey. The required sample size is 1,260 patients from 50 hospitals across Thailand. Each of the hospital will enroll 10 to 40 consecutive patients, depending on case availability on the date conducting the survey, with dyslipidemia and classified as high risk as defined by the protocol. Lipid levels will be based on serological analysis conducted by a local laboratory.

For the second phase, each subject will be followed for survival status at 36 months after enrollment. Such follow-up will be done by searching the Thai National Vital Event Registration Database using subjects' Population Identification Number. All activities regarding case selection and data collection will be done by well trained clinical research associates (CRAs). The CRAs are from Khon Kaen University where the Statistical Coordinating Center (SCC) for this project is based and are independent of the investigator. Random auditing visits will also be performed by auditors independent of the SCC. These are to ensure not only high quality data but also protecting right and well being of subjects.


Recruitment information / eligibility

Status Completed
Enrollment 1240
Est. completion date November 2011
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Evidence of high cardiovascular risk

- Dyslipidemic currently being treated with the same therapy for at least 3 months

Exclusion Criteria:

- Recent major trauma(within 12 weeks)

- Recent surgery requiring anesthesia including coronary bypass graft(within 12 weeks)

- Acute or abrupt change(within 1 month) in usual diet

- Pregnancy, breast-feeding currently, or postpartum within the last 6 months

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Thailand Research Site Ban Pong Ratchaburi
Thailand Research Site Hatyai Songkhla
Thailand Research Site Kannayao Bangkok
Thailand Research Site Maung Chachoengsao
Thailand Research Site Maung Chainat
Thailand Research Site Maung Chantaburi
Thailand Research Site Maung Chiang Mai
Thailand Research Site Maung Chumphon
Thailand Research Site Maung Kamphaeng Phet H
Thailand Research Site Maung Kanchanaburi
Thailand Research Site Maung Krabi
Thailand Research Site Maung Lampang
Thailand Research Site Maung Lamphun
Thailand Research Site Maung Lopburi
Thailand Research Site Maung Mahasarakarm
Thailand Research Site Maung Nakorn Nayok
Thailand Research Site Maung Nan
Thailand Research Site Maung Nokhon Si Thammarat
Thailand Research Site Maung Nokorn Pathom
Thailand Research Site Maung Ratchaburi
Thailand Research Site Maung Rayong
Thailand Research Site Maung Roi Et
Thailand Research Site Maung Samut Sakhon
Thailand Research Site Maung Samut songkhram
Thailand Research Site Maung Satun
Thailand Research Site Maung Sisaket
Thailand Research Site Maung Nonthaburi
Thailand Research Site Maung Phang Nga
Thailand Research Site Maung Phatthalung
Thailand Research Site Maung Phayao
Thailand Research Site Maung Phichit
Thailand Research Site Maung Phitsanulok
Thailand Research Site Maung Phrae
Thailand Research Site Maung Phuket
Thailand Research Site Maung Prachuap Khiri Khan
Thailand Research Site Maung Suphanburi
Thailand Research Site Maung Surat Thani
Thailand Research Site Maung Surin
Thailand Research Site Maung Tak
Thailand Research Site Maung Trang
Thailand Research Site Maung Ubon Ratchathani
Thailand Research Site Maung Udon Thani
Thailand Research Site Maung Uthaithani
Thailand Research Site Maung Uttaradit
Thailand Research Site Maung Ang Thong
Thailand Research Site Maung Ayutthaya
Thailand Research Site Muang Nong Khai
Thailand Research Site Muang Nakhorn Phanom
Thailand Research Site Muang Khon Kaen

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary LDL-cholesterol June2008 No
Secondary Survival June 2011 No
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