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NCT00701454 Clinical Trial

Survey of Thai-Muslim Health Status

Hypertension Clinical Trial

Official title:
Survey of Thai-Muslim Health Status

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00701454
Other study ID # INMU-2006-01
Secondary ID
Status Completed
Phase N/A
First received June 17, 2008
Last updated June 17, 2008
Start date September 2005
Est. completion date April 2006

Study information
Verified date September 2005
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority Thailand: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The purpose of this study was to determine the prevalence and risk factors of diabetes, hypertension, hyperlipidemia among Thai muslim population aged 35-75 years.

Description:

This was a cross-sectional study conducted in Bangkok and surrounding provinces. Approximately 1500 participants were enrolled. Study staff interviewed participants on basic demographic data, health status, physical activities, food frequency and 24-hour recall. Anthropometry (body weight, height, hip and waist circumference) and physical assessment (blood pressure)were measured. Ten milliliters of venous blood was drawn by venipuncture after a 12 h overnight fast for determination of fasting plasma glucose (FPG) and blood lipid concentrations (total cholesterol, triglyceride, and HDL-cholesterol). FPG was measured by the enzymatic colorimetric method with glucose oxidase.21 Total cholesterol was determined by the cholesterol oxidase method and serum triglycerides concentration was determined by standardized enzymatic procedures using glycerol phosphate oxidase assay.22, 23 HDL- cholesterol was measured by enzymatic assays.24 LDL cholesterol was calculated according to the method of Friedwald et al.25 All samples were analyzed when internal quality control met the acceptable criteria. Intra-and inter-assay CVs were 2.01% and 3.01% for FPG, 1.87% and 4.24% for total cholesterol, 0.93% and 11.6% for triacylglycerols, and 0.99% and 1.49% for HDL cholesterol, respectively.

Recruitment information / eligibility
Status Completed
Enrollment 1488
Est. completion date April 2006
Est. primary completion date April 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 35 Years to 95 Years
Eligibility Inclusion Criteria:

- 35 y and older muslim

- free from severe communicable diseases and mental disorders

Exclusion Criteria:

- not able to complete the interviews or obtain blood samples for analysis

Study Design

Observational Model: Ecologic or Community, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Intervention

Other:
• No intervention
No intervention

Locations
Country Name City State
Thailand Institute of Nutrition, Mahidol University Phuttamonthon Nakhon Pathom

Sponsors (1)
Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome
Type Measure Description Time frame Safety issue
Primary prevalence of diabetes, hypertension and hyperlipidemia after a 12 h overnight fast Yes
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